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rs397516357

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516357(A;A)
Make rs397516357(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position55151910
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516357
ebirs397516357
HLIrs397516357
Exacrs397516357
Varsomers397516357
Maprs397516357
PheGenIrs397516357
hapmaprs397516357
1000 genomesrs397516357
hgdprs397516357
ensemblrs397516357
gopubmedrs397516357
geneviewrs397516357
scholarrs397516357
googlers397516357
pharmgkbrs397516357
gwascentralrs397516357
openSNPrs397516357
23andMers397516357
23andMe allrs397516357
SNP Nexus

SNPshotrs397516357
SNPdbers397516357
MSV3drs397516357
GWAS Ctlgrs397516357
Max Magnitude0
ClinVar
Risk rs397516357(A;A)
Alt rs397516357(A;A)
Reference rs397516357(G;G)
Significance Pathogenic
Disease Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy not provided
Variation info
Gene TNNI3
CLNDBN Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000019.9:g.55663278C>T
CLNSRC ClinVar
CLNACC RCV000157533.2, RCV000167988.1, RCV000223924.1,