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rs863224990

From SNPedia

Orientationminus
Make rs863224990(-;-)
Make rs863224990(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32823372
GeneDMD
is asnp
is mentioned by
dbSNPrs863224990
ebirs863224990
HLIrs863224990
Exacrs863224990
Varsomers863224990
Maprs863224990
PheGenIrs863224990
hapmaprs863224990
1000 genomesrs863224990
hgdprs863224990
ensemblrs863224990
gopubmedrs863224990
geneviewrs863224990
scholarrs863224990
googlers863224990
pharmgkbrs863224990
gwascentralrs863224990
openSNPrs863224990
23andMers863224990
23andMe allrs863224990
SNP Nexus

SNPshotrs863224990
SNPdbers863224990
MSV3drs863224990
GWAS Ctlgrs863224990
Max Magnitude
ClinVar
Risk rs863224990(;)
Alt rs863224990(;)
Reference rs863224990(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32841489delT
CLNSRC Quest Diagnostics
CLNACC RCV000201106.1,