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rs193922409

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922409(A;A)
Make rs193922409(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position55151905
GeneTNNI3
is asnp
is mentioned by
dbSNPrs193922409
ebirs193922409
HLIrs193922409
Exacrs193922409
Varsomers193922409
Maprs193922409
PheGenIrs193922409
hapmaprs193922409
1000 genomesrs193922409
hgdprs193922409
ensemblrs193922409
gopubmedrs193922409
geneviewrs193922409
scholarrs193922409
googlers193922409
pharmgkbrs193922409
gwascentralrs193922409
openSNPrs193922409
23andMers193922409
23andMe allrs193922409
SNP Nexus

SNPshotrs193922409
SNPdbers193922409
MSV3drs193922409
GWAS Ctlgrs193922409
Max Magnitude0
ClinVar
Risk rs193922409(A,T;A,T)
Alt rs193922409(A,T;A,T)
Reference rs193922409(G;G)
Significance Probable-Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene TNNI3
CLNDBN not specified Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000019.9:g.55663273C>A; NC_000019.9:g.55663273C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000159241.1, RCV000030565.1, RCV000159240.2,