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rs397516454

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516454(G;G)
Make rs397516454(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position201365610
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516454
ebirs397516454
HLIrs397516454
Exacrs397516454
Varsomers397516454
Maprs397516454
PheGenIrs397516454
hapmaprs397516454
1000 genomesrs397516454
hgdprs397516454
ensemblrs397516454
gopubmedrs397516454
geneviewrs397516454
scholarrs397516454
googlers397516454
pharmgkbrs397516454
gwascentralrs397516454
openSNPrs397516454
23andMers397516454
23andMe allrs397516454
SNP Nexus

SNPshotrs397516454
SNPdbers397516454
MSV3drs397516454
GWAS Ctlgrs397516454
Max Magnitude0
ClinVar
Risk rs397516454(G;G)
Alt rs397516454(G;G)
Reference rs397516454(T;T)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201334738A>C
CLNSRC ClinVar
CLNACC RCV000036570.3,