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rs397516464

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516464(A;A)
Make rs397516464(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position201364365
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516464
ebirs397516464
HLIrs397516464
Exacrs397516464
Varsomers397516464
Maprs397516464
PheGenIrs397516464
hapmaprs397516464
1000 genomesrs397516464
hgdprs397516464
ensemblrs397516464
gopubmedrs397516464
geneviewrs397516464
scholarrs397516464
googlers397516464
pharmgkbrs397516464
gwascentralrs397516464
openSNPrs397516464
23andMers397516464
23andMe allrs397516464
SNP Nexus

SNPshotrs397516464
SNPdbers397516464
MSV3drs397516464
GWAS Ctlgrs397516464
Max Magnitude0
ClinVar
Risk rs397516464(A,C;A,C)
Alt rs397516464(A,C;A,C)
Reference rs397516464(G;G)
Significance Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201333493C>G; NC_000001.10:g.201333493C>T
CLNSRC ClinVar
CLNACC RCV000036586.2, RCV000036585.3,