rs4761097

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0448 (13394/29892,GnomAD)
G==0421 (12281/29118,TOPMED)
G==0408 (2044/5008,1000G)
G==0432 (1664/3854,ALSPAC)
G==0445 (1649/3708,TWINSUK)
chr12:84793732 (GRCh38.p7) (12q21.31)
AD
GWASCatalog
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 12NC_000012.12:g.84793732G>A
GRCh37.p13 chr 12NC_000012.11:g.85187511G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.453A=0.547
1000GenomesAmericanSub694G=0.340A=0.660
1000GenomesEast AsianSub1008G=0.213A=0.787
1000GenomesEuropeSub1006G=0.460A=0.540
1000GenomesGlobalStudy-wide5008G=0.408A=0.592
1000GenomesSouth AsianSub978G=0.540A=0.460
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.432A=0.568
The Genome Aggregation DatabaseAfricanSub8694G=0.458A=0.542
The Genome Aggregation DatabaseAmericanSub838G=0.340A=0.660
The Genome Aggregation DatabaseEast AsianSub1620G=0.231A=0.769
The Genome Aggregation DatabaseEuropeSub18440G=0.468A=0.531
The Genome Aggregation DatabaseGlobalStudy-wide29892G=0.448A=0.551
The Genome Aggregation DatabaseOtherSub300G=0.390A=0.610
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.421A=0.578
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.445A=0.555
PMID Title Author Journal
23942779A genome-wide association study of behavioral disinhibition.McGue MBehav Genet

P-Value

SNP ID p-value Traits Study
rs47610972E-06alcohol dependence23942779

eQTL of rs4761097 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 rs4761097 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.