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rs17636733

From SNPedia

Orientationplus
Stabilizedplus
Make rs17636733(C;C)
Make rs17636733(C;T)
Make rs17636733(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position25667192
is asnp
is mentioned by
dbSNPrs17636733
dbSNP (classic)rs17636733
ClinGenrs17636733
ebirs17636733
HLIrs17636733
Exacrs17636733
Gnomadrs17636733
Varsomers17636733
LitVarrs17636733
Maprs17636733
PheGenIrs17636733
Biobankrs17636733
1000 genomesrs17636733
hgdprs17636733
ensemblrs17636733
geneviewrs17636733
scholarrs17636733
googlers17636733
pharmgkbrs17636733
gwascentralrs17636733
openSNPrs17636733
23andMers17636733
SNPshotrs17636733
SNPdbers17636733
MSV3drs17636733
GWAS Ctlgrs17636733
GMAF0.2957
Max Magnitude0
? (C;C) (C;T) (T;T) 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 2E-7
Odds Ratio None None