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rs201366610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201366610(C;C)
Make rs201366610(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32501833
GeneDMD
is asnp
is mentioned by
dbSNPrs201366610
ebirs201366610
HLIrs201366610
Exacrs201366610
Varsomers201366610
Maprs201366610
PheGenIrs201366610
hapmaprs201366610
1000 genomesrs201366610
hgdprs201366610
ensemblrs201366610
gopubmedrs201366610
geneviewrs201366610
scholarrs201366610
googlers201366610
pharmgkbrs201366610
gwascentralrs201366610
openSNPrs201366610
23andMers201366610
23andMe allrs201366610
SNP Nexus

SNPshotrs201366610
SNPdbers201366610
MSV3drs201366610
GWAS Ctlgrs201366610
GMAF0.0006046
Max Magnitude0
ClinVar
Risk rs201366610(A,C;A,C)
Alt rs201366610(A,C;A,C)
Reference rs201366610(G;G)
Significance Pathogenic
Disease Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Reversed 0
HGVS NC_000023.10:g.32519950G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011973.12, RCV000150069.2,