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rs727503255

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503255(C;C)
Make rs727503255(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424977
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503255
ebirs727503255
HLIrs727503255
Exacrs727503255
Varsomers727503255
Maprs727503255
PheGenIrs727503255
hapmaprs727503255
1000 genomesrs727503255
hgdprs727503255
ensemblrs727503255
gopubmedrs727503255
geneviewrs727503255
scholarrs727503255
googlers727503255
pharmgkbrs727503255
gwascentralrs727503255
openSNPrs727503255
23andMers727503255
23andMe allrs727503255
SNP Nexus

SNPshotrs727503255
SNPdbers727503255
MSV3drs727503255
GWAS Ctlgrs727503255
Max Magnitude0
ClinVar
Risk rs727503255(C;C)
Alt rs727503255(C;C)
Reference rs727503255(T;T)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy Hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23894186A>G
CLNSRC
CLNACC RCV000151269.2, RCV000227735.1,