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rs397516345

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516345(C;T)
Make rs397516345(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position55154745
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516345
ebirs397516345
HLIrs397516345
Exacrs397516345
Varsomers397516345
Maprs397516345
PheGenIrs397516345
hapmaprs397516345
1000 genomesrs397516345
hgdprs397516345
ensemblrs397516345
gopubmedrs397516345
geneviewrs397516345
scholarrs397516345
googlers397516345
pharmgkbrs397516345
gwascentralrs397516345
openSNPrs397516345
23andMers397516345
23andMe allrs397516345
SNP Nexus

SNPshotrs397516345
SNPdbers397516345
MSV3drs397516345
GWAS Ctlgrs397516345
Max Magnitude0
ClinVar
Risk rs397516345(T;T)
Alt rs397516345(T;T)
Reference rs397516345(C;C)
Significance Probable-Pathogenic
Disease not specified Cardiomyopathy
Variation info
Gene TNNI3
CLNDBN not specified Cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55666113G>A
CLNSRC
CLNACC RCV000036285.2, RCV000159217.1,