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rs397516461

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516461(A;A)
Make rs397516461(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position201365220
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516461
ebirs397516461
HLIrs397516461
Exacrs397516461
Varsomers397516461
Maprs397516461
PheGenIrs397516461
hapmaprs397516461
1000 genomesrs397516461
hgdprs397516461
ensemblrs397516461
gopubmedrs397516461
geneviewrs397516461
scholarrs397516461
googlers397516461
pharmgkbrs397516461
gwascentralrs397516461
openSNPrs397516461
23andMers397516461
23andMe allrs397516461
SNP Nexus

SNPshotrs397516461
SNPdbers397516461
MSV3drs397516461
GWAS Ctlgrs397516461
Max Magnitude0
ClinVar
Risk rs397516461(A;A)
Alt rs397516461(A;A)
Reference rs397516461(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201334348C>T
CLNSRC ClinVar
CLNACC RCV000036581.2,