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rs863224975

From SNPedia

Orientationminus
Make rs863224975(-;-)
Make rs863224975(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31178759
GeneDMD
is asnp
is mentioned by
dbSNPrs863224975
ebirs863224975
HLIrs863224975
Exacrs863224975
Varsomers863224975
Maprs863224975
PheGenIrs863224975
hapmaprs863224975
1000 genomesrs863224975
hgdprs863224975
ensemblrs863224975
gopubmedrs863224975
geneviewrs863224975
scholarrs863224975
googlers863224975
pharmgkbrs863224975
gwascentralrs863224975
openSNPrs863224975
23andMers863224975
23andMe allrs863224975
SNP Nexus

SNPshotrs863224975
SNPdbers863224975
MSV3drs863224975
GWAS Ctlgrs863224975
Max Magnitude
ClinVar
Risk rs863224975(;)
Alt rs863224975(;)
Reference rs863224975(A;A)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31196876delT
CLNSRC Quest Diagnostics
CLNACC RCV000201110.1,