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rs1064793986

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position32454778
GeneDMD
is asnp
is mentioned by
dbSNPrs1064793986
dbSNP (old)rs1064793986
ClinGenrs1064793986
ebirs1064793986
HLIrs1064793986
Exacrs1064793986
Gnomadrs1064793986
Varsomers1064793986
Maprs1064793986
PheGenIrs1064793986
Biobankrs1064793986
1000 genomesrs1064793986
hgdprs1064793986
ensemblrs1064793986
gopubmedrs1064793986
geneviewrs1064793986
scholarrs1064793986
googlers1064793986
pharmgkbrs1064793986
gwascentralrs1064793986
openSNPrs1064793986
23andMers1064793986
23andMe allrs1064793986
SNPshotrs1064793986
SNPdbers1064793986
MSV3drs1064793986
GWAS Ctlgrs1064793986
Max Magnitude0
ClinVar
Risk rs1064793986(T;T)
Alt rs1064793986(T;T)
Reference Rs1064793986(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32472895G>A
CLNSRC
CLNACC RCV000482346.1,