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rs727503864

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503864(C;T)
Make rs727503864(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position32697947
GeneDMD
is asnp
is mentioned by
dbSNPrs727503864
ebirs727503864
HLIrs727503864
Exacrs727503864
Varsomers727503864
Maprs727503864
PheGenIrs727503864
hapmaprs727503864
1000 genomesrs727503864
hgdprs727503864
ensemblrs727503864
gopubmedrs727503864
geneviewrs727503864
scholarrs727503864
googlers727503864
pharmgkbrs727503864
gwascentralrs727503864
openSNPrs727503864
23andMers727503864
23andMe allrs727503864
SNP Nexus

SNPshotrs727503864
SNPdbers727503864
MSV3drs727503864
GWAS Ctlgrs727503864
Max Magnitude0
ClinVar
Risk rs727503864(T;T)
Alt rs727503864(T;T)
Reference rs727503864(C;C)
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.32716064G>A
CLNSRC HGMD
CLNACC RCV000153011.3, RCV000153012.3, RCV000153013.3,