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rs762860653

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs762860653(C;C)
Make rs762860653(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32501767
GeneDMD
is asnp
is mentioned by
dbSNPrs762860653
ebirs762860653
HLIrs762860653
Exacrs762860653
Varsomers762860653
Maprs762860653
PheGenIrs762860653
hapmaprs762860653
1000 genomesrs762860653
hgdprs762860653
ensemblrs762860653
gopubmedrs762860653
geneviewrs762860653
scholarrs762860653
googlers762860653
pharmgkbrs762860653
gwascentralrs762860653
openSNPrs762860653
23andMers762860653
23andMe allrs762860653
SNP Nexus

SNPshotrs762860653
SNPdbers762860653
MSV3drs762860653
GWAS Ctlgrs762860653
Max Magnitude0
ClinVar
Risk rs762860653(C;C)
Alt rs762860653(C;C)
Reference rs762860653(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 0
HGVS NC_000023.10:g.32519884G>A
CLNSRC Quest Diagnostics
CLNACC RCV000201099.1,