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rs1057520764

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520764(C;T)
Make rs1057520764(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32342264
GeneDMD
is asnp
is mentioned by
dbSNPrs1057520764
dbSNP (old)rs1057520764
ClinGenrs1057520764
ebirs1057520764
HLIrs1057520764
Exacrs1057520764
Gnomadrs1057520764
Varsomers1057520764
Maprs1057520764
PheGenIrs1057520764
Biobankrs1057520764
1000 genomesrs1057520764
hgdprs1057520764
ensemblrs1057520764
gopubmedrs1057520764
geneviewrs1057520764
scholarrs1057520764
googlers1057520764
pharmgkbrs1057520764
gwascentralrs1057520764
openSNPrs1057520764
23andMers1057520764
23andMe allrs1057520764
SNPshotrs1057520764
SNPdbers1057520764
MSV3drs1057520764
GWAS Ctlgrs1057520764
Max Magnitude0
ClinVar
Risk rs1057520764(T;T)
Alt rs1057520764(T;T)
Reference Rs1057520764(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32360381G>A
CLNSRC
CLNACC RCV000424485.1,