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rs397516355

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516355(A;A)
Make rs397516355(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position55154035
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516355
ebirs397516355
HLIrs397516355
Exacrs397516355
Varsomers397516355
Maprs397516355
PheGenIrs397516355
hapmaprs397516355
1000 genomesrs397516355
hgdprs397516355
ensemblrs397516355
gopubmedrs397516355
geneviewrs397516355
scholarrs397516355
googlers397516355
pharmgkbrs397516355
gwascentralrs397516355
openSNPrs397516355
23andMers397516355
23andMe allrs397516355
SNP Nexus

SNPshotrs397516355
SNPdbers397516355
MSV3drs397516355
GWAS Ctlgrs397516355
Max Magnitude0
ClinVar
Risk rs397516355(A;A)
Alt rs397516355(A;A)
Reference rs397516355(G;G)
Significance Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene TNNI3
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 1
HGVS NC_000019.9:g.55665403C>T
CLNSRC ClinVar
CLNACC RCV000036303.2, RCV000159235.1,