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rs863225001

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225001(C;T)
Make rs863225001(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32364605
GeneDMD
is asnp
is mentioned by
dbSNPrs863225001
ebirs863225001
HLIrs863225001
Exacrs863225001
Varsomers863225001
Maprs863225001
PheGenIrs863225001
hapmaprs863225001
1000 genomesrs863225001
hgdprs863225001
ensemblrs863225001
gopubmedrs863225001
geneviewrs863225001
scholarrs863225001
googlers863225001
pharmgkbrs863225001
gwascentralrs863225001
openSNPrs863225001
23andMers863225001
23andMe allrs863225001
SNP Nexus

SNPshotrs863225001
SNPdbers863225001
MSV3drs863225001
GWAS Ctlgrs863225001
Max Magnitude0
ClinVar
Risk rs863225001(T;T)
Alt rs863225001(T;T)
Reference rs863225001(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32382722G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201095.1,