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rs1057519180

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057519180(-;G)
Make rs1057519180(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position33020152
GeneDMD
is asnp
is mentioned by
dbSNPrs1057519180
dbSNP (old)rs1057519180
ClinGenrs1057519180
ebirs1057519180
HLIrs1057519180
Exacrs1057519180
Gnomadrs1057519180
Varsomers1057519180
Maprs1057519180
PheGenIrs1057519180
Biobankrs1057519180
1000 genomesrs1057519180
hgdprs1057519180
ensemblrs1057519180
gopubmedrs1057519180
geneviewrs1057519180
scholarrs1057519180
googlers1057519180
pharmgkbrs1057519180
gwascentralrs1057519180
openSNPrs1057519180
23andMers1057519180
23andMe allrs1057519180
SNPshotrs1057519180
SNPdbers1057519180
MSV3drs1057519180
GWAS Ctlgrs1057519180
Max Magnitude0
ClinVar
Risk rs1057519180(G;G)
Alt rs1057519180(G;G)
Reference Rs1057519180(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.33038270dupC
CLNSRC
CLNACC RCV000415825.1,