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rs863225102

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225102(A;A)
Make rs863225102(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position23425414
GeneMYH7
is asnp
is mentioned by
dbSNPrs863225102
ebirs863225102
HLIrs863225102
Exacrs863225102
Varsomers863225102
Maprs863225102
PheGenIrs863225102
hapmaprs863225102
1000 genomesrs863225102
hgdprs863225102
ensemblrs863225102
gopubmedrs863225102
geneviewrs863225102
scholarrs863225102
googlers863225102
pharmgkbrs863225102
gwascentralrs863225102
openSNPrs863225102
23andMers863225102
23andMe allrs863225102
SNP Nexus

SNPshotrs863225102
SNPdbers863225102
MSV3drs863225102
GWAS Ctlgrs863225102
Max Magnitude0
ClinVar
Risk rs863225102(A;A)
Alt rs863225102(A;A)
Reference rs863225102(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.23894623A>T
CLNSRC
CLNACC RCV000201493.1,