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rs727503850

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503850(A;T)
Make rs727503850(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position32484967
GeneDMD
is asnp
is mentioned by
dbSNPrs727503850
ebirs727503850
HLIrs727503850
Exacrs727503850
Varsomers727503850
Maprs727503850
PheGenIrs727503850
hapmaprs727503850
1000 genomesrs727503850
hgdprs727503850
ensemblrs727503850
gopubmedrs727503850
geneviewrs727503850
scholarrs727503850
googlers727503850
pharmgkbrs727503850
gwascentralrs727503850
openSNPrs727503850
23andMers727503850
23andMe allrs727503850
SNP Nexus

SNPshotrs727503850
SNPdbers727503850
MSV3drs727503850
GWAS Ctlgrs727503850
Max Magnitude0
ClinVar
Risk rs727503850(T;T)
Alt rs727503850(T;T)
Reference rs727503850(A;A)
Significance Pathogenic
Disease Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32503084T>A
CLNSRC
CLNACC RCV000152962.3, RCV000152963.3, RCV000152964.3,