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rs797044743

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044743(-;GTTT)
Make rs797044743(GTTT;GTTT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position31932168
GeneDMD
is asnp
is mentioned by
dbSNPrs797044743
ClinGenrs797044743
ebirs797044743
HLIrs797044743
Exacrs797044743
Varsomers797044743
Maprs797044743
PheGenIrs797044743
hapmaprs797044743
1000 genomesrs797044743
hgdprs797044743
ensemblrs797044743
gopubmedrs797044743
geneviewrs797044743
scholarrs797044743
googlers797044743
pharmgkbrs797044743
gwascentralrs797044743
openSNPrs797044743
23andMers797044743
23andMe allrs797044743
SNP Nexus

SNPshotrs797044743
SNPdbers797044743
MSV3drs797044743
GWAS Ctlgrs797044743
Max Magnitude0
ClinVar
Risk rs797044743(GTTT;GTTT)
Alt rs797044743(GTTT;GTTT)
Reference Rs797044743(;)
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.31950285_31950286insAAAC
CLNSRC
CLNACC RCV000178600.1, RCV000178601.1,