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rs373286166

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373286166(C;T)
Make rs373286166(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position32573529
GeneDMD
is asnp
is mentioned by
dbSNPrs373286166
ebirs373286166
HLIrs373286166
Exacrs373286166
Varsomers373286166
Maprs373286166
PheGenIrs373286166
hapmaprs373286166
1000 genomesrs373286166
hgdprs373286166
ensemblrs373286166
gopubmedrs373286166
geneviewrs373286166
scholarrs373286166
googlers373286166
pharmgkbrs373286166
gwascentralrs373286166
openSNPrs373286166
23andMers373286166
23andMe allrs373286166
SNP Nexus

SNPshotrs373286166
SNPdbers373286166
MSV3drs373286166
GWAS Ctlgrs373286166
Max Magnitude0
ClinVar
Risk rs373286166(T;T)
Alt rs373286166(T;T)
Reference rs373286166(C;C)
Significance Pathogenic
Disease Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 0
HGVS NC_000023.10:g.32591646C>T
CLNSRC Quest Diagnostics
CLNACC RCV000149882.1, RCV000201160.1,