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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
dbSNP (classic)rs13415097
ClinGenrs13415097
ebirs13415097
HLIrs13415097
Exacrs13415097
Gnomadrs13415097
Varsomers13415097
LitVarrs13415097
Maprs13415097
PheGenIrs13415097
Biobankrs13415097
1000 genomesrs13415097
hgdprs13415097
ensemblrs13415097
geneviewrs13415097
scholarrs13415097
googlers13415097
pharmgkbrs13415097
gwascentralrs13415097
openSNPrs13415097
23andMers13415097
SNPshotrs13415097
SNPdbers13415097
MSV3drs13415097
GWAS Ctlgrs13415097
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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


[PMID 32220223OA-icon.png] Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcification.