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rs1064796764

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position32348405
GeneDMD
is asnp
is mentioned by
dbSNPrs1064796764
dbSNP (classic)rs1064796764
ClinGenrs1064796764
ebirs1064796764
HLIrs1064796764
Exacrs1064796764
Gnomadrs1064796764
Varsomers1064796764
LitVarrs1064796764
Maprs1064796764
PheGenIrs1064796764
Biobankrs1064796764
1000 genomesrs1064796764
hgdprs1064796764
ensemblrs1064796764
geneviewrs1064796764
scholarrs1064796764
googlers1064796764
pharmgkbrs1064796764
gwascentralrs1064796764
openSNPrs1064796764
23andMers1064796764
23andMe allrs1064796764
SNPshotrs1064796764
SNPdbers1064796764
MSV3drs1064796764
GWAS Ctlgrs1064796764
Max Magnitude0
ClinVar
Risk rs1064796764(A;A)
Alt rs1064796764(A;A)
Reference Rs1064796764(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.32366522C>T
CLNSRC
CLNACC RCV000487293.1,