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rs1064792967

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(ACC;ACC) 0 common in clinvar
ChromosomeX
Position31820041
GeneDMD
is asnp
is mentioned by
dbSNPrs1064792967
dbSNP (old)rs1064792967
ClinGenrs1064792967
ebirs1064792967
HLIrs1064792967
Exacrs1064792967
Gnomadrs1064792967
Varsomers1064792967
Maprs1064792967
PheGenIrs1064792967
Biobankrs1064792967
1000 genomesrs1064792967
hgdprs1064792967
ensemblrs1064792967
gopubmedrs1064792967
geneviewrs1064792967
scholarrs1064792967
googlers1064792967
pharmgkbrs1064792967
gwascentralrs1064792967
openSNPrs1064792967
23andMers1064792967
23andMe allrs1064792967
SNPshotrs1064792967
SNPdbers1064792967
MSV3drs1064792967
GWAS Ctlgrs1064792967
Max Magnitude0
ClinVar
Risk rs1064792967(GTTT;GTTT)
Alt rs1064792967(GTTT;GTTT)
Reference Rs1064792967(ACC;ACC)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31838158_31838160delGGTinsAAAC
CLNSRC
CLNACC RCV000461452.1,