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rs727503858

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503858(G;G)
Make rs727503858(G;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position32491415
GeneDMD
is asnp
is mentioned by
dbSNPrs727503858
ebirs727503858
HLIrs727503858
Exacrs727503858
Varsomers727503858
Maprs727503858
PheGenIrs727503858
hapmaprs727503858
1000 genomesrs727503858
hgdprs727503858
ensemblrs727503858
gopubmedrs727503858
geneviewrs727503858
scholarrs727503858
googlers727503858
pharmgkbrs727503858
gwascentralrs727503858
openSNPrs727503858
23andMers727503858
23andMe allrs727503858
SNP Nexus

SNPshotrs727503858
SNPdbers727503858
MSV3drs727503858
GWAS Ctlgrs727503858
Max Magnitude0
ClinVar
Risk rs727503858(G;G)
Alt rs727503858(G;G)
Reference rs727503858(T;T)
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.32509532A>C
CLNSRC
CLNACC RCV000152999.3, RCV000153000.3, RCV000153001.3,