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rs193922382

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs193922382(C;T)
Make rs193922382(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position47334002
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs193922382
ebirs193922382
HLIrs193922382
Exacrs193922382
Varsomers193922382
Maprs193922382
PheGenIrs193922382
hapmaprs193922382
1000 genomesrs193922382
hgdprs193922382
ensemblrs193922382
gopubmedrs193922382
geneviewrs193922382
scholarrs193922382
googlers193922382
pharmgkbrs193922382
gwascentralrs193922382
openSNPrs193922382
23andMers193922382
23andMe allrs193922382
SNP Nexus

SNPshotrs193922382
SNPdbers193922382
MSV3drs193922382
GWAS Ctlgrs193922382
Max Magnitude0
ClinVar
Risk rs193922382(T;T)
Alt rs193922382(T;T)
Reference rs193922382(C;C)
Significance Probable-non-pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene MYBPC3
CLNDBN Primary familial hypertrophic cardiomyopathy not specified
Reversed 1
HGVS NC_000011.9:g.47355553G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030287.1, RCV000035542.2,