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rs863225097

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225097(A;C)
Make rs863225097(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23425780
GeneMYH7
is asnp
is mentioned by
dbSNPrs863225097
ebirs863225097
HLIrs863225097
Exacrs863225097
Varsomers863225097
Maprs863225097
PheGenIrs863225097
hapmaprs863225097
1000 genomesrs863225097
hgdprs863225097
ensemblrs863225097
gopubmedrs863225097
geneviewrs863225097
scholarrs863225097
googlers863225097
pharmgkbrs863225097
gwascentralrs863225097
openSNPrs863225097
23andMers863225097
23andMe allrs863225097
SNP Nexus

SNPshotrs863225097
SNPdbers863225097
MSV3drs863225097
GWAS Ctlgrs863225097
Max Magnitude0
ClinVar
Risk rs863225097(C;C)
Alt rs863225097(C;C)
Reference rs863225097(A;A)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23894989T>G
CLNSRC
CLNACC RCV000201480.1,