rs10936425

Homo sapiens
A>G
LINC01324 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0132 (3965/29918,GnomAD)
G=0169 (4929/29118,TOPMED)
G=0142 (712/5008,1000G)
G=0104 (400/3854,ALSPAC)
G=0107 (395/3708,TWINSUK)
chr3:164816238 (GRCh38.p7) (3q26.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 3NC_000003.12:g.164816238A>G
GRCh37.p13 chr 3NC_000003.11:g.164534026A>G

Gene: LINC01324, long intergenic non-protein coding RNA 1324(minus strand)

Molecule type Change Amino acid[Codon] SO Term
LINC01324 transcriptNR_126405.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.745G=0.255
1000GenomesAmericanSub694A=0.920G=0.080
1000GenomesEast AsianSub1008A=0.905G=0.095
1000GenomesEuropeSub1006A=0.906G=0.094
1000GenomesGlobalStudy-wide5008A=0.858G=0.142
1000GenomesSouth AsianSub978A=0.870G=0.130
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.896G=0.104
The Genome Aggregation DatabaseAfricanSub8678A=0.758G=0.242
The Genome Aggregation DatabaseAmericanSub838A=0.940G=0.060
The Genome Aggregation DatabaseEast AsianSub1614A=0.898G=0.102
The Genome Aggregation DatabaseEuropeSub18488A=0.912G=0.087
The Genome Aggregation DatabaseGlobalStudy-wide29918A=0.867G=0.132
The Genome Aggregation DatabaseOtherSub300A=0.910G=0.090
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.830G=0.169
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.893G=0.107
PMID Title Author Journal
24962325Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families.Kapoor MDrug Alcohol Depend

P-Value

SNP ID p-value Traits Study
rs109364256.06E-08alcohol dependence (age at onset)24962325

eQTL of rs10936425 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 rs10936425 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.