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rs193922387

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAA;GAA) 0 common in clinvar
Make rs193922387(-;-)
Make rs193922387(-;GAA)
ReferenceGRCh38 38.1/141
Chromosome14
Position23424794
GeneMYH7
is asnp
is mentioned by
dbSNPrs193922387
ebirs193922387
HLIrs193922387
Exacrs193922387
Varsomers193922387
Maprs193922387
PheGenIrs193922387
hapmaprs193922387
1000 genomesrs193922387
hgdprs193922387
ensemblrs193922387
gopubmedrs193922387
geneviewrs193922387
scholarrs193922387
googlers193922387
pharmgkbrs193922387
gwascentralrs193922387
openSNPrs193922387
23andMers193922387
23andMe allrs193922387
SNP Nexus

SNPshotrs193922387
SNPdbers193922387
MSV3drs193922387
GWAS Ctlgrs193922387
Max Magnitude0
ClinVar
Risk rs193922387(;)
Alt rs193922387(;)
Reference rs193922387(GAA;GAA)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23894003_23894005delTTC
CLNSRC ClinVar
CLNACC RCV000030315.1,