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rs1064794569

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position31507280
GeneDMD
is asnp
is mentioned by
dbSNPrs1064794569
dbSNP (old)rs1064794569
ClinGenrs1064794569
ebirs1064794569
HLIrs1064794569
Exacrs1064794569
Gnomadrs1064794569
Varsomers1064794569
LitVarrs1064794569
Maprs1064794569
PheGenIrs1064794569
Biobankrs1064794569
1000 genomesrs1064794569
hgdprs1064794569
ensemblrs1064794569
gopubmedrs1064794569
geneviewrs1064794569
scholarrs1064794569
googlers1064794569
pharmgkbrs1064794569
gwascentralrs1064794569
openSNPrs1064794569
23andMers1064794569
23andMe allrs1064794569
SNPshotrs1064794569
SNPdbers1064794569
MSV3drs1064794569
GWAS Ctlgrs1064794569
Max Magnitude0
ClinVar
Risk rs1064794569(A;A)
Alt rs1064794569(A;A)
Reference Rs1064794569(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.31525397C>T
CLNSRC
CLNACC RCV000485023.1,