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rs397516344

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516344(C;T)
Make rs397516344(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position55154806
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516344
ebirs397516344
HLIrs397516344
Exacrs397516344
Varsomers397516344
Maprs397516344
PheGenIrs397516344
hapmaprs397516344
1000 genomesrs397516344
hgdprs397516344
ensemblrs397516344
gopubmedrs397516344
geneviewrs397516344
scholarrs397516344
googlers397516344
pharmgkbrs397516344
gwascentralrs397516344
openSNPrs397516344
23andMers397516344
23andMe allrs397516344
SNP Nexus

SNPshotrs397516344
SNPdbers397516344
MSV3drs397516344
GWAS Ctlgrs397516344
Max Magnitude0
ClinVar
Risk rs397516344(T;T)
Alt rs397516344(T;T)
Reference rs397516344(C;C)
Significance Probable-Pathogenic
Disease not specified Hypertrophic cardiomyopathy
Variation info
Gene TNNI3
CLNDBN not specified Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55666174G>A; NC_000019.9:g.55666174G>C
CLNSRC ClinVar
CLNACC RCV000036283.3, RCV000198680.1,