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rs777864641

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777864641(C;T)
Make rs777864641(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32348504
GeneDMD
is asnp
is mentioned by
dbSNPrs777864641
ebirs777864641
HLIrs777864641
Exacrs777864641
Varsomers777864641
Maprs777864641
PheGenIrs777864641
hapmaprs777864641
1000 genomesrs777864641
hgdprs777864641
ensemblrs777864641
gopubmedrs777864641
geneviewrs777864641
scholarrs777864641
googlers777864641
pharmgkbrs777864641
gwascentralrs777864641
openSNPrs777864641
23andMers777864641
23andMe allrs777864641
SNP Nexus

SNPshotrs777864641
SNPdbers777864641
MSV3drs777864641
GWAS Ctlgrs777864641
Max Magnitude0
ClinVar
Risk rs777864641(T;T)
Alt rs777864641(T;T)
Reference rs777864641(C;C)
Significance Pathogenic
Disease Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy
Reversed 0
HGVS NC_000023.10:g.32366621C>A
CLNSRC Quest Diagnostics
CLNACC RCV000201039.1,