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rs863225095

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225095(A;A)
Make rs863225095(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23424793
GeneMYH7
is asnp
is mentioned by
dbSNPrs863225095
ebirs863225095
HLIrs863225095
Exacrs863225095
Varsomers863225095
Maprs863225095
PheGenIrs863225095
hapmaprs863225095
1000 genomesrs863225095
hgdprs863225095
ensemblrs863225095
gopubmedrs863225095
geneviewrs863225095
scholarrs863225095
googlers863225095
pharmgkbrs863225095
gwascentralrs863225095
openSNPrs863225095
23andMers863225095
23andMe allrs863225095
SNP Nexus

SNPshotrs863225095
SNPdbers863225095
MSV3drs863225095
GWAS Ctlgrs863225095
Max Magnitude0
ClinVar
Risk rs863225095(A;A)
Alt rs863225095(A;A)
Reference rs863225095(T;T)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23894002A>T
CLNSRC
CLNACC RCV000201496.1,