rs1471450

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
G==0294 (8803/29858,GnomAD)
G==0246 (7171/29116,TOPMED)
G==0374 (1875/5008,1000G)
chr13:54670721 (GRCh38.p7) (13q14.3)
AD
GWASCatalog
1   publication(s)
See rs on genome
0 Enhancer around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 13NC_000013.11:g.54670721G>A
GRCh37.p13 chr 13NC_000013.10:g.55244856G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.043A=0.957
1000GenomesAmericanSub694G=0.400A=0.600
1000GenomesEast AsianSub1008G=0.710A=0.290
1000GenomesEuropeSub1006G=0.340A=0.660
1000GenomesGlobalStudy-wide5008G=0.374A=0.626
1000GenomesSouth AsianSub978G=0.500A=0.500
The Genome Aggregation DatabaseAfricanSub8714G=0.087A=0.913
The Genome Aggregation DatabaseAmericanSub836G=0.390A=0.610
The Genome Aggregation DatabaseEast AsianSub1608G=0.733A=0.267
The Genome Aggregation DatabaseEuropeSub18398G=0.350A=0.650
The Genome Aggregation DatabaseGlobalStudy-wide29858G=0.294A=0.705
The Genome Aggregation DatabaseOtherSub302G=0.320A=0.680
Trans-Omics for Precision MedicineGlobalStudy-wide29116G=0.246A=0.753
PMID Title Author Journal
29071344Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression.Zhou HJAMA Psychiatry

P-Value

SNP ID p-value Traits Study
rs14714502E-06alcohol dependence29071344

eQTL of rs1471450 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 rs1471450 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.