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rs1064793644

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
ChromosomeX
Position31209690
GeneDMD
is asnp
is mentioned by
dbSNPrs1064793644
dbSNP (old)rs1064793644
ClinGenrs1064793644
ebirs1064793644
HLIrs1064793644
Exacrs1064793644
Gnomadrs1064793644
Varsomers1064793644
Maprs1064793644
PheGenIrs1064793644
Biobankrs1064793644
1000 genomesrs1064793644
hgdprs1064793644
ensemblrs1064793644
gopubmedrs1064793644
geneviewrs1064793644
scholarrs1064793644
googlers1064793644
pharmgkbrs1064793644
gwascentralrs1064793644
openSNPrs1064793644
23andMers1064793644
23andMe allrs1064793644
SNPshotrs1064793644
SNPdbers1064793644
MSV3drs1064793644
GWAS Ctlgrs1064793644
Max Magnitude0
ClinVar
Risk rs1064793644(-;-)
Alt rs1064793644(-;-)
Reference Rs1064793644(TT;TT)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.31227807_31227808delAA
CLNSRC
CLNACC RCV000480017.1,