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rs193922389

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922389(A;C)
Make rs193922389(C;C)
ReferenceGRCh38 38.1/141
Chromosome14
Position23419555
GeneMYH7
is asnp
is mentioned by
dbSNPrs193922389
ebirs193922389
HLIrs193922389
Exacrs193922389
Varsomers193922389
Maprs193922389
PheGenIrs193922389
hapmaprs193922389
1000 genomesrs193922389
hgdprs193922389
ensemblrs193922389
gopubmedrs193922389
geneviewrs193922389
scholarrs193922389
googlers193922389
pharmgkbrs193922389
gwascentralrs193922389
openSNPrs193922389
23andMers193922389
23andMe allrs193922389
SNP Nexus

SNPshotrs193922389
SNPdbers193922389
MSV3drs193922389
GWAS Ctlgrs193922389
Max Magnitude0
ClinVar
Risk rs193922389(C;C)
Alt rs193922389(C;C)
Reference rs193922389(A;A)
Significance Probable-Pathogenic
Disease Cardiomyopathy
Variation info
Gene MYH7 MIR208B
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23888764T>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030317.1,