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rs727503253

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503253(C;T)
Make rs727503253(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424119
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503253
ebirs727503253
HLIrs727503253
Exacrs727503253
Varsomers727503253
Maprs727503253
PheGenIrs727503253
hapmaprs727503253
1000 genomesrs727503253
hgdprs727503253
ensemblrs727503253
gopubmedrs727503253
geneviewrs727503253
scholarrs727503253
googlers727503253
pharmgkbrs727503253
gwascentralrs727503253
openSNPrs727503253
23andMers727503253
23andMe allrs727503253
SNP Nexus

SNPshotrs727503253
SNPdbers727503253
MSV3drs727503253
GWAS Ctlgrs727503253
Max Magnitude0
ClinVar
Risk rs727503253(T;T)
Alt rs727503253(T;T)
Reference rs727503253(C;C)
Significance Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23893328G>A
CLNSRC
CLNACC RCV000208124.2,