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rs727503844

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503844(C;T)
Make rs727503844(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position32468704
GeneDMD
is asnp
is mentioned by
dbSNPrs727503844
ebirs727503844
HLIrs727503844
Exacrs727503844
Varsomers727503844
Maprs727503844
PheGenIrs727503844
hapmaprs727503844
1000 genomesrs727503844
hgdprs727503844
ensemblrs727503844
gopubmedrs727503844
geneviewrs727503844
scholarrs727503844
googlers727503844
pharmgkbrs727503844
gwascentralrs727503844
openSNPrs727503844
23andMers727503844
23andMe allrs727503844
SNP Nexus

SNPshotrs727503844
SNPdbers727503844
MSV3drs727503844
GWAS Ctlgrs727503844
Max Magnitude0
ClinVar
Risk rs727503844(T;T)
Alt rs727503844(T;T)
Reference rs727503844(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy Becker muscular dystrophy Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Becker muscular dystrophy Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32486821G>A
CLNSRC HGMD
CLNACC RCV000152954.3, RCV000152955.3, RCV000176399.1,