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rs17659543

From SNPedia

Orientationplus
Stabilizedplus
Make rs17659543(C;C)
Make rs17659543(C;T)
Make rs17659543(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position112958729
is asnp
is mentioned by
dbSNPrs17659543
dbSNP (classic)rs17659543
ClinGenrs17659543
ebirs17659543
HLIrs17659543
Exacrs17659543
Gnomadrs17659543
Varsomers17659543
LitVarrs17659543
Maprs17659543
PheGenIrs17659543
Biobankrs17659543
1000 genomesrs17659543
hgdprs17659543
ensemblrs17659543
geneviewrs17659543
scholarrs17659543
googlers17659543
pharmgkbrs17659543
gwascentralrs17659543
openSNPrs17659543
23andMers17659543
SNPshotrs17659543
SNPdbers17659543
MSV3drs17659543
GWAS Ctlgrs17659543
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 24903972] Genetic predisposition to calcific aortic stenosis and mitral annular calcification