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rs863224978

From SNPedia

Orientationminus
Make rs863224978(-;-)
Make rs863224978(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32644315
GeneDMD
is asnp
is mentioned by
dbSNPrs863224978
ebirs863224978
HLIrs863224978
Exacrs863224978
Varsomers863224978
Maprs863224978
PheGenIrs863224978
hapmaprs863224978
1000 genomesrs863224978
hgdprs863224978
ensemblrs863224978
gopubmedrs863224978
geneviewrs863224978
scholarrs863224978
googlers863224978
pharmgkbrs863224978
gwascentralrs863224978
openSNPrs863224978
23andMers863224978
23andMe allrs863224978
SNP Nexus

SNPshotrs863224978
SNPdbers863224978
MSV3drs863224978
GWAS Ctlgrs863224978
Max Magnitude
ClinVar
Risk rs863224978(;)
Alt rs863224978(;)
Reference rs863224978(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32662432delT
CLNSRC Quest Diagnostics
CLNACC RCV000201205.1,