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rs1057518207

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518207(A;A)
Make rs1057518207(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position32545158
GeneDMD
is asnp
is mentioned by
dbSNPrs1057518207
dbSNP (old)rs1057518207
ClinGenrs1057518207
ebirs1057518207
HLIrs1057518207
Exacrs1057518207
Gnomadrs1057518207
Varsomers1057518207
Maprs1057518207
PheGenIrs1057518207
Biobankrs1057518207
1000 genomesrs1057518207
hgdprs1057518207
ensemblrs1057518207
gopubmedrs1057518207
geneviewrs1057518207
scholarrs1057518207
googlers1057518207
pharmgkbrs1057518207
gwascentralrs1057518207
openSNPrs1057518207
23andMers1057518207
23andMe allrs1057518207
SNPshotrs1057518207
SNPdbers1057518207
MSV3drs1057518207
GWAS Ctlgrs1057518207
Max Magnitude0
ClinVar
Risk rs1057518207(A;A)
Alt rs1057518207(A;A)
Reference Rs1057518207(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32563275C>T
CLNSRC
CLNACC RCV000414740.1,