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rs193922388

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922388(A;A)
Make rs193922388(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position23420234
GeneMYH7
is asnp
is mentioned by
dbSNPrs193922388
ebirs193922388
HLIrs193922388
Exacrs193922388
Varsomers193922388
Maprs193922388
PheGenIrs193922388
hapmaprs193922388
1000 genomesrs193922388
hgdprs193922388
ensemblrs193922388
gopubmedrs193922388
geneviewrs193922388
scholarrs193922388
googlers193922388
pharmgkbrs193922388
gwascentralrs193922388
openSNPrs193922388
23andMers193922388
23andMe allrs193922388
SNP Nexus

SNPshotrs193922388
SNPdbers193922388
MSV3drs193922388
GWAS Ctlgrs193922388
Max Magnitude0
ClinVar
Risk rs193922388(A;A)
Alt rs193922388(A;A)
Reference rs193922388(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 1
HGVS NC_000014.8:g.23889443C>T
CLNSRC ClinVar LabCorp
CLNACC RCV000030316.1, RCV000158603.2,