rs9301980

Homo sapiens
T>A / T>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0113 (3402/29958,GnomAD)
G=0136 (3968/29118,TOPMED)
G=0108 (541/5008,1000G)
G=0104 (400/3854,ALSPAC)
G=0104 (384/3708,TWINSUK)
chr13:87091772 (GRCh38.p7) (13q31.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.87091772T>A
GRCh38.p7 chr 13NC_000013.11:g.87091772T>G
GRCh37.p13 chr 13NC_000013.10:g.87744027T>A
GRCh37.p13 chr 13NC_000013.10:g.87744027T>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322T=0.818G=0.182
1000GenomesAmericanSub694T=0.920G=0.080
1000GenomesEast AsianSub1008T=0.968G=0.032
1000GenomesEuropeSub1006T=0.906G=0.094
1000GenomesGlobalStudy-wide5008T=0.892G=0.108
1000GenomesSouth AsianSub978T=0.880G=0.120
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.896G=0.104
The Genome Aggregation DatabaseAfricanSub8706T=0.813G=0.187
The Genome Aggregation DatabaseAmericanSub838T=0.920G=0.080
The Genome Aggregation DatabaseEast AsianSub1622T=0.954G=0.046
The Genome Aggregation DatabaseEuropeSub18490T=0.913G=0.086
The Genome Aggregation DatabaseGlobalStudy-wide29958T=0.886G=0.113
The Genome Aggregation DatabaseOtherSub302T=0.850G=0.150
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.863G=0.136
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.896G=0.104
PMID Title Author Journal
23743675A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.Kapoor MHum Genet

P-Value

SNP ID p-value Traits Study
rs93019800.000127alcohol consumption23743675

eQTL of rs9301980 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 rs9301980 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.