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rs146071084

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs146071084(A;T)
Make rs146071084(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32454660
GeneDMD
is asnp
is mentioned by
dbSNPrs146071084
ebirs146071084
HLIrs146071084
Exacrs146071084
Varsomers146071084
Maprs146071084
PheGenIrs146071084
hapmaprs146071084
1000 genomesrs146071084
hgdprs146071084
ensemblrs146071084
gopubmedrs146071084
geneviewrs146071084
scholarrs146071084
googlers146071084
pharmgkbrs146071084
gwascentralrs146071084
openSNPrs146071084
23andMers146071084
23andMe allrs146071084
SNP Nexus

SNPshotrs146071084
SNPdbers146071084
MSV3drs146071084
GWAS Ctlgrs146071084
Max Magnitude0
ClinVar
Risk rs146071084(T;T)
Alt rs146071084(T;T)
Reference rs146071084(A;A)
Significance Pathogenic
Disease not provided Duchenne muscular dystrophy Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN not provided Duchenne muscular dystrophy Becker muscular dystrophy
Reversed 0
HGVS NC_000023.10:g.32472777A>T
CLNSRC
CLNACC RCV000080587.3, RCV000176660.1, RCV000176661.1,