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rs863224985

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224985(G;T)
Make rs863224985(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32518085
GeneDMD
is asnp
is mentioned by
dbSNPrs863224985
ebirs863224985
HLIrs863224985
Exacrs863224985
Varsomers863224985
Maprs863224985
PheGenIrs863224985
hapmaprs863224985
1000 genomesrs863224985
hgdprs863224985
ensemblrs863224985
gopubmedrs863224985
geneviewrs863224985
scholarrs863224985
googlers863224985
pharmgkbrs863224985
gwascentralrs863224985
openSNPrs863224985
23andMers863224985
23andMe allrs863224985
SNP Nexus

SNPshotrs863224985
SNPdbers863224985
MSV3drs863224985
GWAS Ctlgrs863224985
Max Magnitude0
ClinVar
Risk rs863224985(T;T)
Alt rs863224985(T;T)
Reference rs863224985(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32536202C>A
CLNSRC Quest Diagnostics
CLNACC RCV000201007.1,