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rs770845480

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs770845480(C;C)
Make rs770845480(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32346023
GeneDMD
is asnp
is mentioned by
dbSNPrs770845480
ebirs770845480
HLIrs770845480
Exacrs770845480
Varsomers770845480
Maprs770845480
PheGenIrs770845480
hapmaprs770845480
1000 genomesrs770845480
hgdprs770845480
ensemblrs770845480
gopubmedrs770845480
geneviewrs770845480
scholarrs770845480
googlers770845480
pharmgkbrs770845480
gwascentralrs770845480
openSNPrs770845480
23andMers770845480
23andMe allrs770845480
SNP Nexus

SNPshotrs770845480
SNPdbers770845480
MSV3drs770845480
GWAS Ctlgrs770845480
Max Magnitude0
ClinVar
Risk rs770845480(C;C)
Alt rs770845480(C;C)
Reference rs770845480(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 0
HGVS NC_000023.10:g.32364140G>A
CLNSRC
CLNACC RCV000229638.1,