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rs128627256

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs128627256(C;T)
Make rs128627256(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31478330
GeneDMD
is asnp
is mentioned by
dbSNPrs128627256
ebirs128627256
HLIrs128627256
Exacrs128627256
Varsomers128627256
Maprs128627256
PheGenIrs128627256
hapmaprs128627256
1000 genomesrs128627256
hgdprs128627256
ensemblrs128627256
gopubmedrs128627256
geneviewrs128627256
scholarrs128627256
googlers128627256
pharmgkbrs128627256
gwascentralrs128627256
openSNPrs128627256
23andMers128627256
23andMe allrs128627256
SNP Nexus

SNPshotrs128627256
SNPdbers128627256
MSV3drs128627256
GWAS Ctlgrs128627256
Max Magnitude0
OMIM300377
Desc
Variant0082
Relatedalso
ClinVar
Risk rs128627256(T;T)
Alt rs128627256(T;T)
Reference rs128627256(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy Dilated cardiomyopathy 3B Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Dilated cardiomyopathy 3B Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31496447G>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000012040.5, RCV000150057.3, RCV000179221.1,