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rs397516341

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516341(A;G)
Make rs397516341(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position55157589
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516341
ebirs397516341
HLIrs397516341
Exacrs397516341
Varsomers397516341
Maprs397516341
PheGenIrs397516341
hapmaprs397516341
1000 genomesrs397516341
hgdprs397516341
ensemblrs397516341
gopubmedrs397516341
geneviewrs397516341
scholarrs397516341
googlers397516341
pharmgkbrs397516341
gwascentralrs397516341
openSNPrs397516341
23andMers397516341
23andMe allrs397516341
SNP Nexus

SNPshotrs397516341
SNPdbers397516341
MSV3drs397516341
GWAS Ctlgrs397516341
Max Magnitude0
ClinVar
Risk rs397516341(G;G)
Alt rs397516341(G;G)
Reference rs397516341(A;A)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene TNNI3
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55668957T>C
CLNSRC ClinVar
CLNACC RCV000036273.2,