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rs397516356

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516356(A;A)
Make rs397516356(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position55151917
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516356
ebirs397516356
HLIrs397516356
Exacrs397516356
Varsomers397516356
Maprs397516356
PheGenIrs397516356
hapmaprs397516356
1000 genomesrs397516356
hgdprs397516356
ensemblrs397516356
gopubmedrs397516356
geneviewrs397516356
scholarrs397516356
googlers397516356
pharmgkbrs397516356
gwascentralrs397516356
openSNPrs397516356
23andMers397516356
23andMe allrs397516356
SNP Nexus

SNPshotrs397516356
SNPdbers397516356
MSV3drs397516356
GWAS Ctlgrs397516356
Max Magnitude0
ClinVar
Risk rs397516356(A;A)
Alt rs397516356(A;A)
Reference rs397516356(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TNNI3
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55663285C>T
CLNSRC ClinVar
CLNACC RCV000036305.3,