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rs13038095

From SNPedia

Orientationplus
Stabilizedplus
Make rs13038095(G;G)
Make rs13038095(G;T)
Make rs13038095(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position47796832
is asnp
is mentioned by
dbSNPrs13038095
ebirs13038095
HLIrs13038095
Exacrs13038095
Varsomers13038095
Maprs13038095
PheGenIrs13038095
hapmaprs13038095
1000 genomesrs13038095
hgdprs13038095
ensemblrs13038095
gopubmedrs13038095
geneviewrs13038095
scholarrs13038095
googlers13038095
pharmgkbrs13038095
gwascentralrs13038095
openSNPrs13038095
23andMers13038095
23andMe allrs13038095
SNP Nexus

SNPshotrs13038095
SNPdbers13038095
MSV3drs13038095
GWAS Ctlgrs13038095
GMAF0.1042
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20173747OA-icon.png]
Trait Atrial fibrillation
Title Common variants in KCNN3 are associated with lone atrial fibrillation
Risk Allele
P-val 2E-7
Odds Ratio 1.47 [1.39-1.54]