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rs397516450

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516450(A;G)
Make rs397516450(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position201365656
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516450
ebirs397516450
HLIrs397516450
Exacrs397516450
Varsomers397516450
Maprs397516450
PheGenIrs397516450
hapmaprs397516450
1000 genomesrs397516450
hgdprs397516450
ensemblrs397516450
gopubmedrs397516450
geneviewrs397516450
scholarrs397516450
googlers397516450
pharmgkbrs397516450
gwascentralrs397516450
openSNPrs397516450
23andMers397516450
23andMe allrs397516450
SNP Nexus

SNPshotrs397516450
SNPdbers397516450
MSV3drs397516450
GWAS Ctlgrs397516450
Max Magnitude0
ClinVar
Risk rs397516450(G;G)
Alt rs397516450(G;G)
Reference rs397516450(A;A)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201334784T>C
CLNSRC ClinVar
CLNACC RCV000036562.2,