rs371403

Homo sapiens
A>G
None
Check p-value
SNV (Single Nucleotide Variation)
G=0179 (5383/29934,GnomAD)
G=0164 (4797/29118,TOPMED)
G=0120 (603/5008,1000G)
G=0265 (1020/3854,ALSPAC)
G=0268 (994/3708,TWINSUK)
chr6:52937446 (GRCh38.p7) (6p12.2)
AD
GWASdb2
1   publication(s)
See rs on genome
6 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 6NC_000006.12:g.52937446A>G
GRCh37.p13 chr 6NC_000006.11:g.52802244A>G

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.970G=0.030
1000GenomesAmericanSub694A=0.830G=0.170
1000GenomesEast AsianSub1008A=0.959G=0.041
1000GenomesEuropeSub1006A=0.724G=0.276
1000GenomesGlobalStudy-wide5008A=0.880G=0.120
1000GenomesSouth AsianSub978A=0.870G=0.130
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.735G=0.265
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.835G=0.164
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.732G=0.268
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
rs3714030.000778alcohol dependence21314694

eQTL of rs371403 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 rs371403 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 )
chr65280216252802252E0700
chr65275856352758844E071-43400
chr65284111452841240E07138870
chr65275751952757904E074-44340
chr65275798452758450E074-43794
chr65275856352758844E074-43400