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rs1057524291

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524291(C;T)
Make rs1057524291(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32411763
GeneDMD
is asnp
is mentioned by
dbSNPrs1057524291
dbSNP (old)rs1057524291
ClinGenrs1057524291
ebirs1057524291
HLIrs1057524291
Exacrs1057524291
Gnomadrs1057524291
Varsomers1057524291
Maprs1057524291
PheGenIrs1057524291
Biobankrs1057524291
1000 genomesrs1057524291
hgdprs1057524291
ensemblrs1057524291
gopubmedrs1057524291
geneviewrs1057524291
scholarrs1057524291
googlers1057524291
pharmgkbrs1057524291
gwascentralrs1057524291
openSNPrs1057524291
23andMers1057524291
23andMe allrs1057524291
SNPshotrs1057524291
SNPdbers1057524291
MSV3drs1057524291
GWAS Ctlgrs1057524291
Max Magnitude0
ClinVar
Risk rs1057524291(T;T)
Alt rs1057524291(T;T)
Reference Rs1057524291(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32429880G>A
CLNSRC
CLNACC RCV000430460.1,