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rs863225000

From SNPedia

Orientationminus
Make rs863225000(-;-)
Make rs863225000(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32365127
GeneDMD
is asnp
is mentioned by
dbSNPrs863225000
ebirs863225000
HLIrs863225000
Exacrs863225000
Varsomers863225000
Maprs863225000
PheGenIrs863225000
hapmaprs863225000
1000 genomesrs863225000
hgdprs863225000
ensemblrs863225000
gopubmedrs863225000
geneviewrs863225000
scholarrs863225000
googlers863225000
pharmgkbrs863225000
gwascentralrs863225000
openSNPrs863225000
23andMers863225000
23andMe allrs863225000
SNP Nexus

SNPshotrs863225000
SNPdbers863225000
MSV3drs863225000
GWAS Ctlgrs863225000
Max Magnitude
ClinVar
Risk rs863225000(;)
Alt rs863225000(;)
Reference rs863225000(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32383244delT
CLNSRC Quest Diagnostics
CLNACC RCV000201034.1,