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rs797044756

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044756(-;T)
Make rs797044756(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32823360
GeneDMD
is asnp
is mentioned by
dbSNPrs797044756
dbSNP (old)rs797044756
ClinGenrs797044756
ebirs797044756
HLIrs797044756
Exacrs797044756
Gnomadrs797044756
Varsomers797044756
Maprs797044756
PheGenIrs797044756
Biobankrs797044756
1000 genomesrs797044756
hgdprs797044756
ensemblrs797044756
gopubmedrs797044756
geneviewrs797044756
scholarrs797044756
googlers797044756
pharmgkbrs797044756
gwascentralrs797044756
openSNPrs797044756
23andMers797044756
23andMe allrs797044756
SNP Nexus

SNPshotrs797044756
SNPdbers797044756
MSV3drs797044756
GWAS Ctlgrs797044756
Max Magnitude0
ClinVar
Risk rs797044756(T;T)
Alt rs797044756(T;T)
Reference Rs797044756(-;-)
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.32841478dupA
CLNSRC
CLNACC RCV000178886.1, RCV000178887.1,