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rs863225098

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225098(A;A)
Make rs863225098(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23420213
GeneMYH7
is asnp
is mentioned by
dbSNPrs863225098
ebirs863225098
HLIrs863225098
Exacrs863225098
Varsomers863225098
Maprs863225098
PheGenIrs863225098
hapmaprs863225098
1000 genomesrs863225098
hgdprs863225098
ensemblrs863225098
gopubmedrs863225098
geneviewrs863225098
scholarrs863225098
googlers863225098
pharmgkbrs863225098
gwascentralrs863225098
openSNPrs863225098
23andMers863225098
23andMe allrs863225098
SNP Nexus

SNPshotrs863225098
SNPdbers863225098
MSV3drs863225098
GWAS Ctlgrs863225098
Max Magnitude0
ClinVar
Risk rs863225098(A;A)
Alt rs863225098(A;A)
Reference rs863225098(G;G)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23889422C>T
CLNSRC
CLNACC RCV000201510.1,