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rs13415097

From SNPedia

Orientationplus
Stabilizedplus
Make rs13415097(C;C)
Make rs13415097(C;T)
Make rs13415097(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position112959608
is asnp
is mentioned by
dbSNPrs13415097
ebirs13415097
HLIrs13415097
Exacrs13415097
Varsomers13415097
Maprs13415097
PheGenIrs13415097
hapmaprs13415097
1000 genomesrs13415097
hgdprs13415097
ensemblrs13415097
gopubmedrs13415097
geneviewrs13415097
scholarrs13415097
googlers13415097
pharmgkbrs13415097
gwascentralrs13415097
openSNPrs13415097
23andMers13415097
23andMe allrs13415097
SNP Nexus

SNPshotrs13415097
SNPdbers13415097
MSV3drs13415097
GWAS Ctlgrs13415097
Max Magnitude
? (C;C) (C;T) (T;T) 28

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