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rs1064793964

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position32491344
GeneDMD
is asnp
is mentioned by
dbSNPrs1064793964
dbSNP (old)rs1064793964
ClinGenrs1064793964
ebirs1064793964
HLIrs1064793964
Exacrs1064793964
Gnomadrs1064793964
Varsomers1064793964
Maprs1064793964
PheGenIrs1064793964
Biobankrs1064793964
1000 genomesrs1064793964
hgdprs1064793964
ensemblrs1064793964
gopubmedrs1064793964
geneviewrs1064793964
scholarrs1064793964
googlers1064793964
pharmgkbrs1064793964
gwascentralrs1064793964
openSNPrs1064793964
23andMers1064793964
23andMe allrs1064793964
SNPshotrs1064793964
SNPdbers1064793964
MSV3drs1064793964
GWAS Ctlgrs1064793964
Max Magnitude0
ClinVar
Risk rs1064793964(A;A)
Alt rs1064793964(A;A)
Reference Rs1064793964(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32509461C>T
CLNSRC
CLNACC RCV000483792.1,