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rs727503264

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503264(A;C)
Make rs727503264(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23426852
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503264
ebirs727503264
HLIrs727503264
Exacrs727503264
Varsomers727503264
Maprs727503264
PheGenIrs727503264
hapmaprs727503264
1000 genomesrs727503264
hgdprs727503264
ensemblrs727503264
gopubmedrs727503264
geneviewrs727503264
scholarrs727503264
googlers727503264
pharmgkbrs727503264
gwascentralrs727503264
openSNPrs727503264
23andMers727503264
23andMe allrs727503264
SNP Nexus

SNPshotrs727503264
SNPdbers727503264
MSV3drs727503264
GWAS Ctlgrs727503264
Max Magnitude0
ClinVar
Risk rs727503264(C;C)
Alt rs727503264(C;C)
Reference rs727503264(A;A)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23896061T>G
CLNSRC
CLNACC RCV000151284.1,