Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516455

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516455(A;C)
Make rs397516455(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position201365617
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516455
ebirs397516455
HLIrs397516455
Exacrs397516455
Varsomers397516455
Maprs397516455
PheGenIrs397516455
hapmaprs397516455
1000 genomesrs397516455
hgdprs397516455
ensemblrs397516455
gopubmedrs397516455
geneviewrs397516455
scholarrs397516455
googlers397516455
pharmgkbrs397516455
gwascentralrs397516455
openSNPrs397516455
23andMers397516455
23andMe allrs397516455
SNP Nexus

SNPshotrs397516455
SNPdbers397516455
MSV3drs397516455
GWAS Ctlgrs397516455
Max Magnitude0
ClinVar
Risk rs397516455(C;C)
Alt rs397516455(C;C)
Reference rs397516455(A;A)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201334745T>G
CLNSRC ClinVar
CLNACC RCV000036571.2,