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rs1064793479

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GTGA;GTGA) 0 common in clinvar
ChromosomeX
Position32386443
GeneDMD
is asnp
is mentioned by
dbSNPrs1064793479
dbSNP (old)rs1064793479
ClinGenrs1064793479
ebirs1064793479
HLIrs1064793479
Exacrs1064793479
Gnomadrs1064793479
Varsomers1064793479
Maprs1064793479
PheGenIrs1064793479
Biobankrs1064793479
1000 genomesrs1064793479
hgdprs1064793479
ensemblrs1064793479
gopubmedrs1064793479
geneviewrs1064793479
scholarrs1064793479
googlers1064793479
pharmgkbrs1064793479
gwascentralrs1064793479
openSNPrs1064793479
23andMers1064793479
23andMe allrs1064793479
SNPshotrs1064793479
SNPdbers1064793479
MSV3drs1064793479
GWAS Ctlgrs1064793479
Max Magnitude0
ClinVar
Risk rs1064793479(-;-)
Alt rs1064793479(-;-)
Reference Rs1064793479(GTGA;GTGA)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32404560_32404563delTCAC
CLNSRC
CLNACC RCV000484535.1,