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rs397516347

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516347(A;A)
Make rs397516347(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position55154157
GeneTNNI3
is asnp
is mentioned by
dbSNPrs397516347
ebirs397516347
HLIrs397516347
Exacrs397516347
Varsomers397516347
Maprs397516347
PheGenIrs397516347
hapmaprs397516347
1000 genomesrs397516347
hgdprs397516347
ensemblrs397516347
gopubmedrs397516347
geneviewrs397516347
scholarrs397516347
googlers397516347
pharmgkbrs397516347
gwascentralrs397516347
openSNPrs397516347
23andMers397516347
23andMe allrs397516347
SNP Nexus

SNPshotrs397516347
SNPdbers397516347
MSV3drs397516347
GWAS Ctlgrs397516347
Max Magnitude0
ClinVar
Risk rs397516347(A;A)
Alt rs397516347(A;A)
Reference rs397516347(G;G)
Significance Other
Disease Familial hypertrophic cardiomyopathy 7 not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene TNNI3
CLNDBN Familial hypertrophic cardiomyopathy 7 not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000019.9:g.55665525C>T
CLNSRC ClinVar
CLNACC RCV000036290.4, RCV000159220.2, RCV000211743.1,