rs13356385

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0084 (2514/29822,GnomAD)
A=0128 (3751/29118,TOPMED)
A=0093 (466/5008,1000G)
A=0001 (2/3854,ALSPAC)
A=0000 (0/3708,TWINSUK)
chr5:122234922 (GRCh38.p7) (5q23.2)
AD
GWASdb2
1   publication(s)
See rs on genome
6 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 5NC_000005.10:g.122234922G>A
GRCh37.p13 chr 5NC_000005.9:g.121570617G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.660A=0.340
1000GenomesAmericanSub694G=0.980A=0.020
1000GenomesEast AsianSub1008G=1.000A=0.000
1000GenomesEuropeSub1006G=0.998A=0.002
1000GenomesGlobalStudy-wide5008G=0.907A=0.093
1000GenomesSouth AsianSub978G=1.000A=0.000
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.999A=0.001
The Genome Aggregation DatabaseAfricanSub8640G=0.712A=0.288
The Genome Aggregation DatabaseAmericanSub826G=0.980A=0.020
The Genome Aggregation DatabaseEast AsianSub1606G=1.000A=0.000
The Genome Aggregation DatabaseEuropeSub18448G=0.999A=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29822G=0.915A=0.084
The Genome Aggregation DatabaseOtherSub302G=1.000A=0.000
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.871A=0.128
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=1.000A=0.000
PMID Title Author Journal
21314694Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.Kendler KSAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs133563858.85E-05alcohol dependence21314694

eQTL of rs13356385 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 rs13356385 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 )
chr5121599158121599609E07028541
chr5121599646121599721E07029029
chr5121600267121600370E07029650
chr5121531920121531970E071-38647
chr5121534872121535222E082-35395
chr5121536321121536430E082-34187