rs2881345

Homo sapiens
C>A / C>T
None
Check p-value
SNV (Single Nucleotide Variation)
A=0300 (8980/29886,GnomAD)
A=0399 (11638/29118,TOPMED)
A=0311 (1556/5008,1000G)
A=0135 (521/3854,ALSPAC)
A=0150 (557/3708,TWINSUK)
chr14:57201005 (GRCh38.p7) (14q22.3)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 14NC_000014.9:g.57201005C>A
GRCh38.p7 chr 14NC_000014.9:g.57201005C>T
GRCh37.p13 chr 14NC_000014.8:g.57667723C>A
GRCh37.p13 chr 14NC_000014.8:g.57667723C>T

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322C=0.154A=0.846
1000GenomesAmericanSub694C=0.870A=0.130
1000GenomesEast AsianSub1008C=0.886A=0.114
1000GenomesEuropeSub1006C=0.882A=0.118
1000GenomesGlobalStudy-wide5008C=0.689A=0.311
1000GenomesSouth AsianSub978C=0.880A=0.120
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.865A=0.135
The Genome Aggregation DatabaseAfricanSub8702C=0.279T=0.000
The Genome Aggregation DatabaseAmericanSub836C=0.890T=0.00,
The Genome Aggregation DatabaseEast AsianSub1612C=0.855T=0.000
The Genome Aggregation DatabaseEuropeSub18434C=0.873T=0.000
The Genome Aggregation DatabaseGlobalStudy-wide29886C=0.699T=0.000
The Genome Aggregation DatabaseOtherSub302C=0.850T=0.00,
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.600A=0.399
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=0.850A=0.150
PMID Title Author Journal
23743675A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.Kapoor MHum Genet

P-Value

SNP ID p-value Traits Study
rs28813457.7E-05alcohol consumption23743675

eQTL of rs2881345 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 rs2881345 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.