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rs104894791

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894791(C;T)
Make rs104894791(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position31177932
GeneDMD
is asnp
is mentioned by
dbSNPrs104894791
ebirs104894791
HLIrs104894791
Exacrs104894791
Varsomers104894791
Maprs104894791
PheGenIrs104894791
hapmaprs104894791
1000 genomesrs104894791
hgdprs104894791
ensemblrs104894791
gopubmedrs104894791
geneviewrs104894791
scholarrs104894791
googlers104894791
pharmgkbrs104894791
gwascentralrs104894791
openSNPrs104894791
23andMers104894791
23andMe allrs104894791
SNP Nexus

SNPshotrs104894791
SNPdbers104894791
MSV3drs104894791
GWAS Ctlgrs104894791
Max Magnitude0
OMIM300377
Desc
Variant0070
Relatedalso
ClinVar
Risk rs104894791(T;T)
Alt rs104894791(T;T)
Reference rs104894791(C;C)
Significance Pathogenic
Disease Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31196049G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012027.9,