rs7795531

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0142 (4248/29926,GnomAD)
T=0175 (5106/29118,TOPMED)
T=0131 (658/5008,1000G)
T=0056 (214/3854,ALSPAC)
T=0070 (258/3708,TWINSUK)
chr7:153171421 (GRCh38.p7) (7q36.2)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 7NC_000007.14:g.153171421C>T
GRCh37.p13 chr 7NC_000007.13:g.152868506C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.646T=0.354
1000GenomesAmericanSub694C=0.910T=0.090
1000GenomesEast AsianSub1008C=0.997T=0.003
1000GenomesEuropeSub1006C=0.931T=0.069
1000GenomesGlobalStudy-wide5008C=0.869T=0.131
1000GenomesSouth AsianSub978C=0.940T=0.060
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.944T=0.056
The Genome Aggregation DatabaseAfricanSub8690C=0.665T=0.335
The Genome Aggregation DatabaseAmericanSub838C=0.930T=0.070
The Genome Aggregation DatabaseEast AsianSub1620C=0.997T=0.003
The Genome Aggregation DatabaseEuropeSub18478C=0.931T=0.068
The Genome Aggregation DatabaseGlobalStudy-wide29926C=0.858T=0.142
The Genome Aggregation DatabaseOtherSub300C=0.960T=0.040
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.824T=0.175
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.930T=0.070
PMID Title Author Journal
23953852Genome-wide association studies of maximum number of drinks.Pan YJ Psychiatr Res

P-Value

SNP ID p-value Traits Study
rs77955318.39E-05alcohol consumption23953852

eQTL of rs7795531 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 rs7795531 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.