rs9614670

Homo sapiens
C>T
None
Check p-value
SNV (Single Nucleotide Variation)
T=0171 (5140/29950,GnomAD)
T=0175 (5112/29114,TOPMED)
T=0150 (749/5008,1000G)
T=0207 (799/3854,ALSPAC)
T=0204 (756/3708,TWINSUK)
chr22:45442936 (GRCh38.p7) (22q13.31)
AD
GWASdb2
1   publication(s)
See rs on genome
46 Enhancers around
9 Promoters around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 22NC_000022.11:g.45442936C>T
GRCh37.p13 chr 22NC_000022.10:g.45838817C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.892T=0.108
1000GenomesAmericanSub694C=0.810T=0.190
1000GenomesEast AsianSub1008C=0.845T=0.155
1000GenomesEuropeSub1006C=0.805T=0.195
1000GenomesGlobalStudy-wide5008C=0.850T=0.150
1000GenomesSouth AsianSub978C=0.870T=0.130
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.793T=0.207
The Genome Aggregation DatabaseAfricanSub8724C=0.873T=0.127
The Genome Aggregation DatabaseAmericanSub838C=0.790T=0.210
The Genome Aggregation DatabaseEast AsianSub1612C=0.860T=0.140
The Genome Aggregation DatabaseEuropeSub18476C=0.807T=0.192
The Genome Aggregation DatabaseGlobalStudy-wide29950C=0.828T=0.171
The Genome Aggregation DatabaseOtherSub300C=0.750T=0.250
Trans-Omics for Precision MedicineGlobalStudy-wide29114C=0.824T=0.175
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.796T=0.204
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
rs96146700.000684alcohol dependence20201924

eQTL of rs9614670 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 rs9614670 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.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr224583066345830713E067-8104
chr224583074245830838E067-7979
chr224583097845831220E067-7597
chr224583122345832080E067-6737
chr224581761145817892E068-20925
chr224583074245830838E068-7979
chr224583097845831220E068-7597
chr224583122345832080E068-6737
chr224587128045872211E06832463
chr224583122345832080E069-6737
chr224579565145795902E070-42915
chr224579594545796266E070-42551
chr224583074245830838E071-7979
chr224583097845831220E071-7597
chr224583122345832080E071-6737
chr224587128045872211E07132463
chr224583034545830510E072-8307
chr224583066345830713E072-8104
chr224583074245830838E072-7979
chr224583097845831220E072-7597
chr224583122345832080E072-6737
chr224583122345832080E073-6737
chr224583122345832080E074-6737
chr224587128045872211E07432463
chr224582835145828723E081-10094
chr224582875145828864E081-9953
chr224582956545829629E081-9188
chr224582970945829860E081-8957
chr224582998745830067E081-8750
chr224583122345832080E081-6737
chr224586459845866146E08125781
chr224586618545866235E08127368
chr224586646745866542E08127650
chr224586728045867324E08128463
chr224588774245888645E08148925
chr224582835145828723E082-10094
chr224582875145828864E082-9953
chr224582956545829629E082-9188
chr224582970945829860E082-8957
chr224582998745830067E082-8750
chr224583122345832080E082-6737
chr224583690345837467E082-1350
chr224586430645864530E08225489
chr224586459845866146E08225781
chr224586618545866235E08227368
chr224588774245888645E08248925










Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr224580929145810202E067-28615
chr224580929145810202E068-28615
chr224580929145810202E069-28615
chr224580929145810202E070-28615
chr224580929145810202E071-28615
chr224580929145810202E072-28615
chr224580929145810202E073-28615
chr224580929145810202E074-28615
chr224580929145810202E082-28615