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rs796065333

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796065333(-;T)
Make rs796065333(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32809594
GeneDMD
is asnp
is mentioned by
dbSNPrs796065333
dbSNP (old)rs796065333
ClinGenrs796065333
ebirs796065333
HLIrs796065333
Exacrs796065333
Gnomadrs796065333
Varsomers796065333
Maprs796065333
PheGenIrs796065333
Biobankrs796065333
1000 genomesrs796065333
hgdprs796065333
ensemblrs796065333
gopubmedrs796065333
geneviewrs796065333
scholarrs796065333
googlers796065333
pharmgkbrs796065333
gwascentralrs796065333
openSNPrs796065333
23andMers796065333
23andMe allrs796065333
SNP Nexus

SNPshotrs796065333
SNPdbers796065333
MSV3drs796065333
GWAS Ctlgrs796065333
Max Magnitude0
ClinVar
Risk rs796065333(T;T)
Alt rs796065333(T;T)
Reference Rs796065333(-;-)
Significance Pathogenic
Disease Duchenne muscular dystrophy Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32827712dupA
CLNSRC
CLNACC RCV000179866.1, RCV000179867.1,