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rs193922390

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922390(A;A)
Make rs193922390(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23415651
GeneMYH7
is asnp
is mentioned by
dbSNPrs193922390
ebirs193922390
HLIrs193922390
Exacrs193922390
Varsomers193922390
Maprs193922390
PheGenIrs193922390
hapmaprs193922390
1000 genomesrs193922390
hgdprs193922390
ensemblrs193922390
gopubmedrs193922390
geneviewrs193922390
scholarrs193922390
googlers193922390
pharmgkbrs193922390
gwascentralrs193922390
openSNPrs193922390
23andMers193922390
23andMe allrs193922390
SNP Nexus

SNPshotrs193922390
SNPdbers193922390
MSV3drs193922390
GWAS Ctlgrs193922390
Max Magnitude0
ClinVar
Risk rs193922390(A;A)
Alt rs193922390(A;A)
Reference rs193922390(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified Hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7 MHRT
CLNDBN Primary familial hypertrophic cardiomyopathy not specified Hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23884860C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030320.4, RCV000154172.3, RCV000199234.1, RCV000223711.1,