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rs863225101

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225101(A;G)
Make rs863225101(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23426022
GeneMYH7
is asnp
is mentioned by
dbSNPrs863225101
ebirs863225101
HLIrs863225101
Exacrs863225101
Varsomers863225101
Maprs863225101
PheGenIrs863225101
hapmaprs863225101
1000 genomesrs863225101
hgdprs863225101
ensemblrs863225101
gopubmedrs863225101
geneviewrs863225101
scholarrs863225101
googlers863225101
pharmgkbrs863225101
gwascentralrs863225101
openSNPrs863225101
23andMers863225101
23andMe allrs863225101
SNP Nexus

SNPshotrs863225101
SNPdbers863225101
MSV3drs863225101
GWAS Ctlgrs863225101
Max Magnitude0
ClinVar
Risk rs863225101(G;G)
Alt rs863225101(G;G)
Reference rs863225101(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.23895231T>C
CLNSRC
CLNACC RCV000201487.1,