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rs267606770

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606770(G;T)
Make rs267606770(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32501821
GeneDMD
is asnp
is mentioned by
dbSNPrs267606770
ebirs267606770
HLIrs267606770
Exacrs267606770
Varsomers267606770
Maprs267606770
PheGenIrs267606770
hapmaprs267606770
1000 genomesrs267606770
hgdprs267606770
ensemblrs267606770
gopubmedrs267606770
geneviewrs267606770
scholarrs267606770
googlers267606770
pharmgkbrs267606770
gwascentralrs267606770
openSNPrs267606770
23andMers267606770
23andMe allrs267606770
SNP Nexus

SNPshotrs267606770
SNPdbers267606770
MSV3drs267606770
GWAS Ctlgrs267606770
Max Magnitude0
ClinVar
Risk rs267606770(T;T)
Alt rs267606770(T;T)
Reference rs267606770(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32519938C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011975.17,