rs10848958

Homo sapiens
C>T
LOC105369608 : Non Coding Transcript Variant
Check p-value
SNV (Single Nucleotide Variation)
T=0144 (4332/29946,GnomAD)
T=0112 (3277/29118,TOPMED)
T=0083 (415/5008,1000G)
T=0191 (737/3854,ALSPAC)
T=0203 (753/3708,TWINSUK)
chr12:3921938 (GRCh38.p7) (12p13.32)
AD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 12NC_000012.12:g.3921938C>T
GRCh37.p13 chr 12NC_000012.11:g.4031104C>T

Gene: LOC105369608, uncharacterized LOC105369608(minus strand)

Molecule type Change Amino acid[Codon] SO Term
LOC105369608 transcript variant X1XR_931557.2:n.162...XR_931557.2:n.1627G>AG>ANon Coding Transcript Variant
LOC105369608 transcript variant X2XR_001748965.1:n.N/AGenic Downstream Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.973T=0.027
1000GenomesAmericanSub694C=0.920T=0.080
1000GenomesEast AsianSub1008C=0.990T=0.010
1000GenomesEuropeSub1006C=0.813T=0.187
1000GenomesGlobalStudy-wide5008C=0.917T=0.083
1000GenomesSouth AsianSub978C=0.870T=0.130
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.809T=0.191
The Genome Aggregation DatabaseAfricanSub8722C=0.953T=0.047
The Genome Aggregation DatabaseAmericanSub834C=0.910T=0.090
The Genome Aggregation DatabaseEast AsianSub1618C=0.994T=0.006
The Genome Aggregation DatabaseEuropeSub18470C=0.794T=0.205
The Genome Aggregation DatabaseGlobalStudy-wide29946C=0.855T=0.144
The Genome Aggregation DatabaseOtherSub302C=0.820T=0.180
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.887T=0.112
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.797T=0.203
PMID Title Author Journal
21314694Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.Kendler KSAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs108489580.000381alcohol dependence21314694

eQTL of rs10848958 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs10848958 in Fetal Brain

Probe ID Position Gene beta p-value
There is no meQTL annotation for this SNP

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr1240390874039254E0687983
chr1240393854039753E0688281
chr1240397694039934E0688665
chr1240399744040035E0688870
chr1240400634040237E0688959
chr1239883733988423E070-42681
chr1239884803988750E070-42354
chr1239890473989385E070-41719
chr1239923033992671E070-38433
chr1239927053992776E070-38328
chr1239927853992848E070-38256
chr1239928883992945E070-38159
chr1239934913993549E070-37555
chr1239937483993798E070-37306
chr1239938103993912E070-37192
chr1239953313995402E070-35702
chr1239954323995500E070-35604
chr1239955203995721E070-35383
chr1239958313995906E070-35198
chr1239960303996070E070-35034
chr1239965783996628E070-34476
chr1239968603996910E070-34194
chr1239969383997370E070-33734
chr1239974783997624E070-33480
chr1239979403998104E070-33000
chr1240000294000258E070-30846
chr1240002664000369E070-30735
chr1240005034000684E070-30420
chr1240009294000979E070-30125
chr1240010214001214E070-29890
chr1240013304001383E070-29721
chr1240017044001831E070-29273
chr1240018744002006E070-29098
chr1240055464005804E070-25300
chr1240058734006902E070-24202
chr1240069154007146E070-23958
chr1240091614009215E070-21889
chr1240139774014017E070-17087
chr1240141174014173E070-16931
chr1240276674027721E070-3383
chr1240277714027851E070-3253
chr1240278904027944E070-3160
chr1240281894028239E070-2865
chr1240285564028606E070-2498
chr1240290174029108E070-1996
chr1240310294031125E0700
chr1240311454031254E07041
chr1240320114032067E070907
chr1240321774032446E0701073
chr1240324544032527E0701350
chr1240326294032737E0701525
chr1240329574032997E0701853
chr1240330284033068E0701924
chr1240331684033256E0702064
chr1240332574033325E0702153
chr1240334284033604E0702324
chr1240338684033929E0702764
chr1240339914034041E0702887
chr1240408904041413E0709786
chr1240414334041717E07010329
chr1240421114042211E07011007
chr1240422424042437E07011138
chr1240424504042553E07011346
chr1240426544043035E07011550
chr1240744044074864E07043300
chr1240749354075031E07043831
chr1240751314075295E07044027
chr1240753254075375E07044221
chr1240755524075625E07044448
chr1240756924075950E07044588
chr1240055464005804E071-25300
chr1240058734006902E071-24202
chr1240069154007146E071-23958
chr1239943093995202E074-35902
chr1240294414030624E074-480
chr1239902363990324E081-40780
chr1239903613991085E081-40019
chr1239911263992239E081-38865
chr1239923033992671E081-38433
chr1239927053992776E081-38328
chr1239934913993549E081-37555
chr1239937483993798E081-37306
chr1239938103993912E081-37192
chr1239943093995202E081-35902
chr1240058734006902E081-24202
chr1240069154007146E081-23958
chr1240285564028606E081-2498
chr1240290174029108E081-1996
chr1240294414030624E081-480
chr1240329574032997E0811853
chr1240330284033068E0811924
chr1240331684033256E0812064
chr1240332574033325E0812153
chr1240334284033604E0812324
chr1240374114039030E0816307
chr1240390874039254E0817983
chr1240393854039753E0818281
chr1240397694039934E0818665
chr1240399744040035E0818870
chr1240400634040237E0818959
chr1240403674040421E0819263
chr1240404834040659E0819379
chr1240407424040802E0819638
chr1240408904041413E0819786
chr1240414334041717E08110329
chr1239923033992671E082-38433
chr1239927053992776E082-38328
chr1239927853992848E082-38256
chr1240310294031125E0820
chr1240311454031254E08241
chr1240330284033068E0821924
chr1240331684033256E0822064
chr1240332574033325E0822153
chr1240334284033604E0822324
chr1240374114039030E0826307
chr1240390874039254E0827983
chr1240393854039753E0828281
chr1240397694039934E0828665
chr1240399744040035E0828870
chr1240400634040237E0828959
chr1240403674040421E0829263
chr1240404834040659E0829379
chr1240407424040802E0829638
chr1240408904041413E0829786
chr1240414334041717E08210329






Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr1239812903983067E067-48037
chr1239812903983067E068-48037
chr1239812903983067E069-48037
chr1239812903983067E070-48037
chr1239812903983067E071-48037
chr1239812903983067E072-48037
chr1239812903983067E073-48037
chr1239812903983067E074-48037
chr1239812903983067E081-48037
chr1239812903983067E082-48037