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rs727503278

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503278(C;T)
Make rs727503278(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23432714
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503278
ebirs727503278
HLIrs727503278
Exacrs727503278
Varsomers727503278
Maprs727503278
PheGenIrs727503278
hapmaprs727503278
1000 genomesrs727503278
hgdprs727503278
ensemblrs727503278
gopubmedrs727503278
geneviewrs727503278
scholarrs727503278
googlers727503278
pharmgkbrs727503278
gwascentralrs727503278
openSNPrs727503278
23andMers727503278
23andMe allrs727503278
SNP Nexus

SNPshotrs727503278
SNPdbers727503278
MSV3drs727503278
GWAS Ctlgrs727503278
Max Magnitude0
ClinVar
Risk rs727503278(G,T;G,T)
Alt rs727503278(G,T;G,T)
Reference rs727503278(C;C)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 1 Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN not specified Familial hypertrophic cardiomyopathy 1 Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23901923G>A
CLNSRC Centenary Institute
CLNACC RCV000151313.2, RCV000172887.1, RCV000197008.1,