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rs727503265

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727503265(A;A)
Make rs727503265(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23427889
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503265
ebirs727503265
HLIrs727503265
Exacrs727503265
Varsomers727503265
Maprs727503265
PheGenIrs727503265
hapmaprs727503265
1000 genomesrs727503265
hgdprs727503265
ensemblrs727503265
gopubmedrs727503265
geneviewrs727503265
scholarrs727503265
googlers727503265
pharmgkbrs727503265
gwascentralrs727503265
openSNPrs727503265
23andMers727503265
23andMe allrs727503265
SNP Nexus

SNPshotrs727503265
SNPdbers727503265
MSV3drs727503265
GWAS Ctlgrs727503265
Max Magnitude0
ClinVar
Risk rs727503265(A;A)
Alt rs727503265(A;A)
Reference rs727503265(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene MYH7
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000014.8:g.23897098C>T
CLNSRC
CLNACC RCV000151288.2,