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rs397516352

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516352(C;C)
Make rs397516352(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position55154115
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516352
ebirs397516352
HLIrs397516352
Exacrs397516352
Varsomers397516352
Maprs397516352
PheGenIrs397516352
hapmaprs397516352
1000 genomesrs397516352
hgdprs397516352
ensemblrs397516352
gopubmedrs397516352
geneviewrs397516352
scholarrs397516352
googlers397516352
pharmgkbrs397516352
gwascentralrs397516352
openSNPrs397516352
23andMers397516352
23andMe allrs397516352
SNP Nexus

SNPshotrs397516352
SNPdbers397516352
MSV3drs397516352
GWAS Ctlgrs397516352
Max Magnitude0
ClinVar
Risk rs397516352(C;C)
Alt rs397516352(C;C)
Reference rs397516352(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TNNI3
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55665483A>G
CLNSRC ClinVar
CLNACC RCV000036298.2,