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rs267606771

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606771(G;T)
Make rs267606771(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32448611
GeneDMD
is asnp
is mentioned by
dbSNPrs267606771
ebirs267606771
HLIrs267606771
Exacrs267606771
Varsomers267606771
Maprs267606771
PheGenIrs267606771
hapmaprs267606771
1000 genomesrs267606771
hgdprs267606771
ensemblrs267606771
gopubmedrs267606771
geneviewrs267606771
scholarrs267606771
googlers267606771
pharmgkbrs267606771
gwascentralrs267606771
openSNPrs267606771
23andMers267606771
23andMe allrs267606771
SNP Nexus

SNPshotrs267606771
SNPdbers267606771
MSV3drs267606771
GWAS Ctlgrs267606771
Max Magnitude0
ClinVar
Risk rs267606771(T;T)
Alt rs267606771(T;T)
Reference rs267606771(G;G)
Significance Pathogenic
Disease Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32466728C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012031.17,