rs7710841

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0393 (11745/29876,GnomAD)
T=0422 (12309/29118,TOPMED)
T=0412 (2061/5008,1000G)
T=0362 (1397/3854,ALSPAC)
T=0362 (1341/3708,TWINSUK)
chr5:50349986 (GRCh38.p7) (5q11.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.50349986C>T
GRCh37.p13 chr 5NC_000005.9:g.49645820C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.491T=0.509
1000GenomesAmericanSub694C=0.670T=0.330
1000GenomesEast AsianSub1008C=0.527T=0.473
1000GenomesEuropeSub1006C=0.669T=0.331
1000GenomesGlobalStudy-wide5008C=0.588T=0.412
1000GenomesSouth AsianSub978C=0.640T=0.360
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.638T=0.362
The Genome Aggregation DatabaseAfricanSub8704C=0.478T=0.522
The Genome Aggregation DatabaseAmericanSub836C=0.660T=0.340
The Genome Aggregation DatabaseEast AsianSub1572C=0.482T=0.518
The Genome Aggregation DatabaseEuropeSub18464C=0.674T=0.325
The Genome Aggregation DatabaseGlobalStudy-wide29876C=0.606T=0.393
The Genome Aggregation DatabaseOtherSub300C=0.680T=0.320
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.577T=0.422
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.638T=0.362
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs77108410.0000906alcoholismpha002891
rs77108410.0000906alcohol dependence20201924

eQTL of rs7710841 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 rs7710841 in Fetal Brain

Probe ID Position Gene beta p-value
cg15950743chr5:49708521EMB-0.088830637498681.0654e-35

Genomic View

Chromatin Interaction

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