rs12776254

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0143 (4287/29958,GnomAD)
G=0127 (3709/29118,TOPMED)
G=0114 (570/5008,1000G)
G=0167 (645/3854,ALSPAC)
G=0177 (656/3708,TWINSUK)
chr10:2112668 (GRCh38.p7) (10p15.3)
AD
GWASdb2
2   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 10NC_000010.11:g.2112668A>G
GRCh37.p13 chr 10NC_000010.10:g.2154862A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.924G=0.076
1000GenomesAmericanSub694A=0.840G=0.160
1000GenomesEast AsianSub1008A=0.893G=0.107
1000GenomesEuropeSub1006A=0.836G=0.164
1000GenomesGlobalStudy-wide5008A=0.886G=0.114
1000GenomesSouth AsianSub978A=0.910G=0.090
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.833G=0.167
The Genome Aggregation DatabaseAfricanSub8726A=0.907G=0.093
The Genome Aggregation DatabaseAmericanSub834A=0.840G=0.160
The Genome Aggregation DatabaseEast AsianSub1620A=0.883G=0.117
The Genome Aggregation DatabaseEuropeSub18476A=0.831G=0.168
The Genome Aggregation DatabaseGlobalStudy-wide29958A=0.856G=0.143
The Genome Aggregation DatabaseOtherSub302A=0.880G=0.120
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.872G=0.127
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.823G=0.177
PMID Title Author Journal
21703634A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.Wang KSJ Psychiatr Res
20202923A genome-wide association study of alcohol dependence.Bierut LJProc Natl Acad Sci U S A

P-Value

SNP ID p-value Traits Study
rs127762540.00000182alcohol dependence20202923
rs127762540.0000681alcohol dependence21703634

eQTL of rs12776254 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 rs12776254 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 )
chr1021126742112811E070-42051
chr1021128372112969E070-41893
chr1021315722131642E070-23220
chr1021316852131870E070-22992
chr1021642272164406E0709365
chr1021645722165301E0709710
chr1021703612170562E08115499
chr1021708192170869E08115957
chr1021174092117491E082-37371
chr1021175192117632E082-37230
chr1021176752117729E082-37133
chr1021177352117828E082-37034
chr1021708192170869E08215957
chr1021709112171103E08216049