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rs1057524037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524037(C;C)
Make rs1057524037(C;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position31206610
GeneDMD
is asnp
is mentioned by
dbSNPrs1057524037
dbSNP (classic)rs1057524037
ClinGenrs1057524037
ebirs1057524037
HLIrs1057524037
Exacrs1057524037
Gnomadrs1057524037
Varsomers1057524037
LitVarrs1057524037
Maprs1057524037
PheGenIrs1057524037
Biobankrs1057524037
1000 genomesrs1057524037
hgdprs1057524037
ensemblrs1057524037
geneviewrs1057524037
scholarrs1057524037
googlers1057524037
pharmgkbrs1057524037
gwascentralrs1057524037
openSNPrs1057524037
23andMers1057524037
23andMe allrs1057524037
SNPshotrs1057524037
SNPdbers1057524037
MSV3drs1057524037
GWAS Ctlgrs1057524037
Max Magnitude0
ClinVar
Risk rs1057524037(A;A) rs1057524037(C;C)
Alt rs1057524037(A;A) rs1057524037(C;C)
Reference Rs1057524037(T;T)
Significance Pathogenic
Disease not specified Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN not specified Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31224727A>G; NC_000023.10:g.31224727A>T
CLNSRC
CLNACC RCV000436463.1, RCV000456408.1,