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rs863225103

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225103(A;G)
Make rs863225103(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23424924
GeneMYH7
is asnp
is mentioned by
dbSNPrs863225103
ebirs863225103
HLIrs863225103
Exacrs863225103
Varsomers863225103
Maprs863225103
PheGenIrs863225103
hapmaprs863225103
1000 genomesrs863225103
hgdprs863225103
ensemblrs863225103
gopubmedrs863225103
geneviewrs863225103
scholarrs863225103
googlers863225103
pharmgkbrs863225103
gwascentralrs863225103
openSNPrs863225103
23andMers863225103
23andMe allrs863225103
SNP Nexus

SNPshotrs863225103
SNPdbers863225103
MSV3drs863225103
GWAS Ctlgrs863225103
Max Magnitude0
ClinVar
Risk rs863225103(G;G)
Alt rs863225103(G;G)
Reference rs863225103(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.23894133T>C
CLNSRC
CLNACC RCV000201507.1,