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rs16830359

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs16830359(A;A)
Make rs16830359(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position43130713
is asnp
is mentioned by
dbSNPrs16830359
ebirs16830359
HLIrs16830359
Exacrs16830359
Varsomers16830359
Maprs16830359
PheGenIrs16830359
hapmaprs16830359
1000 genomesrs16830359
hgdprs16830359
ensemblrs16830359
gopubmedrs16830359
geneviewrs16830359
scholarrs16830359
googlers16830359
pharmgkbrs16830359
gwascentralrs16830359
openSNPrs16830359
23andMers16830359
23andMe allrs16830359
SNP Nexus

SNPshotrs16830359
SNPdbers16830359
MSV3drs16830359
GWAS Ctlgrs16830359
GMAF0.05051
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21348951OA-icon.png]
Trait
Title Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality
Risk Allele
P-val 1E-7
Odds Ratio None None