rs7168475

Homo sapiens
A>C / A>G
None
Check p-value
SNV (Single Nucleotide Variation)
C=0183 (5486/29952,GnomAD)
C=0136 (683/5008,1000G)
C=0191 (735/3854,ALSPAC)
C=0200 (741/3708,TWINSUK)
chr15:38668681 (GRCh38.p7) (15q14)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 15NC_000015.10:g.38668681A>C
GRCh38.p7 chr 15NC_000015.10:g.38668681A>G
GRCh37.p13 chr 15NC_000015.9:g.38960882A>C
GRCh37.p13 chr 15NC_000015.9:g.38960882A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.796C=0.204
1000GenomesAmericanSub694A=0.880C=0.12,
1000GenomesEast AsianSub1008A=0.924C=0.074
1000GenomesEuropeSub1006A=0.842C=0.158
1000GenomesGlobalStudy-wide5008A=0.863C=0.136
1000GenomesSouth AsianSub978A=0.900C=0.10,
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.809C=0.191
The Genome Aggregation DatabaseAfricanSub8720A=0.801G=0.000
The Genome Aggregation DatabaseAmericanSub838A=0.870G=0.00,
The Genome Aggregation DatabaseEast AsianSub1614A=0.931G=0.001
The Genome Aggregation DatabaseEuropeSub18478A=0.810G=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29952A=0.816G=0.000
The Genome Aggregation DatabaseOtherSub302A=0.870G=0.00,
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.800C=0.200
PMID Title Author Journal
23089632A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53.Wang JCMol Psychiatry

P-Value

SNP ID p-value Traits Study
rs71684750.00000198alcohol dependence23089632
rs71684750.000466alcohol dependence23089632

eQTL of rs7168475 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 rs7168475 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.