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rs2040862

From SNPedia

Orientationplus
Stabilizedplus
Make rs2040862(C;C)
Make rs2040862(C;T)
Make rs2040862(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position138084300
GeneWNT8A
is asnp
is mentioned by
dbSNPrs2040862
ebirs2040862
HLIrs2040862
Exacrs2040862
Varsomers2040862
Maprs2040862
PheGenIrs2040862
hapmaprs2040862
1000 genomesrs2040862
hgdprs2040862
ensemblrs2040862
gopubmedrs2040862
geneviewrs2040862
scholarrs2040862
googlers2040862
pharmgkbrs2040862
gwascentralrs2040862
openSNPrs2040862
23andMers2040862
23andMe allrs2040862
SNP Nexus

SNPshotrs2040862
SNPdbers2040862
MSV3drs2040862
GWAS Ctlgrs2040862
GMAF0.08127
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22544366OA-icon.png]
Trait
Title Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
Risk Allele T
P-val 3E-7
Odds Ratio 1.1200 None


[PMID 18413325OA-icon.png] Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.