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rs863225006

From SNPedia

Orientationminus
Make rs863225006(-;-)
Make rs863225006(-;ATAG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32287688
GeneDMD
is asnp
is mentioned by
dbSNPrs863225006
ebirs863225006
HLIrs863225006
Exacrs863225006
Varsomers863225006
Maprs863225006
PheGenIrs863225006
hapmaprs863225006
1000 genomesrs863225006
hgdprs863225006
ensemblrs863225006
gopubmedrs863225006
geneviewrs863225006
scholarrs863225006
googlers863225006
pharmgkbrs863225006
gwascentralrs863225006
openSNPrs863225006
23andMers863225006
23andMe allrs863225006
SNP Nexus

SNPshotrs863225006
SNPdbers863225006
MSV3drs863225006
GWAS Ctlgrs863225006
Max Magnitude
ClinVar
Risk rs863225006(;)
Alt rs863225006(;)
Reference rs863225006(ATAG;ATAG)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32305805_32305808delCTAT
CLNSRC Quest Diagnostics
CLNACC RCV000201192.1,