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rs756949497

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs756949497(G;T)
Make rs756949497(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32484925
GeneDMD
is asnp
is mentioned by
dbSNPrs756949497
ebirs756949497
HLIrs756949497
Exacrs756949497
Varsomers756949497
Maprs756949497
PheGenIrs756949497
hapmaprs756949497
1000 genomesrs756949497
hgdprs756949497
ensemblrs756949497
gopubmedrs756949497
geneviewrs756949497
scholarrs756949497
googlers756949497
pharmgkbrs756949497
gwascentralrs756949497
openSNPrs756949497
23andMers756949497
23andMe allrs756949497
SNP Nexus

SNPshotrs756949497
SNPdbers756949497
MSV3drs756949497
GWAS Ctlgrs756949497
Max Magnitude0
ClinVar
Risk rs756949497(T;T)
Alt rs756949497(T;T)
Reference rs756949497(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 0
HGVS NC_000023.10:g.32503042G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201047.1,