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rs146880270

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146880270(C;T)
Make rs146880270(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32438312
GeneDMD
is asnp
is mentioned by
dbSNPrs146880270
ebirs146880270
HLIrs146880270
Exacrs146880270
Varsomers146880270
Maprs146880270
PheGenIrs146880270
hapmaprs146880270
1000 genomesrs146880270
hgdprs146880270
ensemblrs146880270
gopubmedrs146880270
geneviewrs146880270
scholarrs146880270
googlers146880270
pharmgkbrs146880270
gwascentralrs146880270
openSNPrs146880270
23andMers146880270
23andMe allrs146880270
SNP Nexus

SNPshotrs146880270
SNPdbers146880270
MSV3drs146880270
GWAS Ctlgrs146880270
Max Magnitude0
ClinVar
Risk rs146880270(T;T)
Alt rs146880270(T;T)
Reference rs146880270(C;C)
Significance Probable-Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 0
HGVS NC_000023.10:g.32456429C>A
CLNSRC
CLNACC RCV000196412.1,