rs7060195

Homo sapiens
T>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0078 (1631/20776,GnomAD)
G=0106 (400/3775,1000G)
G=0060 (223/3708,TWINSUK)
G=0063 (183/2889,ALSPAC)
chrX:93398386 (GRCh38.p7) (Xq21.32)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr XNC_000023.11:g.93398386T>G
GRCh37.p13 chr XNC_000023.10:g.92653385T>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1003T=0.821G=0.179
1000GenomesAmericanSub524T=0.960G=0.040
1000GenomesEast AsianSub764T=0.930G=0.070
1000GenomesEuropeSub766T=0.950G=0.050
1000GenomesGlobalStudy-wide3775T=0.894G=0.106
1000GenomesSouth AsianSub718T=0.850G=0.150
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide2889T=0.937G=0.063
The Genome Aggregation DatabaseAfricanSub5876T=0.839G=0.161
The Genome Aggregation DatabaseAmericanSub588T=0.970G=0.030
The Genome Aggregation DatabaseEast AsianSub1027T=0.932G=0.068
The Genome Aggregation DatabaseEuropeSub13096T=0.955G=0.044
The Genome Aggregation DatabaseGlobalStudy-wide20776T=0.921G=0.078
The Genome Aggregation DatabaseOtherSub189T=0.920G=0.080
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.940G=0.060
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
rs70601950.000842alcohol dependence20201924

eQTL of rs7060195 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 rs7060195 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.