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rs1057524825

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524825(G;T)
Make rs1057524825(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32342150
GeneDMD
is asnp
is mentioned by
dbSNPrs1057524825
dbSNP (old)rs1057524825
ClinGenrs1057524825
ebirs1057524825
HLIrs1057524825
Exacrs1057524825
Gnomadrs1057524825
Varsomers1057524825
LitVarrs1057524825
Maprs1057524825
PheGenIrs1057524825
Biobankrs1057524825
1000 genomesrs1057524825
hgdprs1057524825
ensemblrs1057524825
gopubmedrs1057524825
geneviewrs1057524825
scholarrs1057524825
googlers1057524825
pharmgkbrs1057524825
gwascentralrs1057524825
openSNPrs1057524825
23andMers1057524825
23andMe allrs1057524825
SNPshotrs1057524825
SNPdbers1057524825
MSV3drs1057524825
GWAS Ctlgrs1057524825
Max Magnitude0
ClinVar
Risk rs1057524825(T;T)
Alt rs1057524825(T;T)
Reference Rs1057524825(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32360267C>A
CLNSRC
CLNACC RCV000431150.1,