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rs863225014

From SNPedia

Orientationminus
Make rs863225014(-;-)
Make rs863225014(-;GA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31444594
GeneDMD
is asnp
is mentioned by
dbSNPrs863225014
ebirs863225014
HLIrs863225014
Exacrs863225014
Varsomers863225014
Maprs863225014
PheGenIrs863225014
hapmaprs863225014
1000 genomesrs863225014
hgdprs863225014
ensemblrs863225014
gopubmedrs863225014
geneviewrs863225014
scholarrs863225014
googlers863225014
pharmgkbrs863225014
gwascentralrs863225014
openSNPrs863225014
23andMers863225014
23andMe allrs863225014
SNP Nexus

SNPshotrs863225014
SNPdbers863225014
MSV3drs863225014
GWAS Ctlgrs863225014
Max Magnitude
ClinVar
Risk rs863225014(;)
Alt rs863225014(;)
Reference rs863225014(GA;GA)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31462711_31462712delTC
CLNSRC Quest Diagnostics
CLNACC RCV000201162.1,