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rs863225018

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225018(-;GTAA)
Make rs863225018(GTAA;GTAA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31182770
GeneDMD
is asnp
is mentioned by
dbSNPrs863225018
ClinGenrs863225018
ebirs863225018
HLIrs863225018
Exacrs863225018
Varsomers863225018
Maprs863225018
PheGenIrs863225018
hapmaprs863225018
1000 genomesrs863225018
hgdprs863225018
ensemblrs863225018
gopubmedrs863225018
geneviewrs863225018
scholarrs863225018
googlers863225018
pharmgkbrs863225018
gwascentralrs863225018
openSNPrs863225018
23andMers863225018
23andMe allrs863225018
SNP Nexus

SNPshotrs863225018
SNPdbers863225018
MSV3drs863225018
GWAS Ctlgrs863225018
Max Magnitude0
ClinVar
Risk rs863225018(GTAA;GTAA)
Alt rs863225018(GTAA;GTAA)
Reference Rs863225018(;)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31200888_31200891dupTTAC
CLNSRC Quest Diagnostics
CLNACC RCV000201198.1,