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rs199774535

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199774535(A;A)
Make rs199774535(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position32348491
GeneDMD
is asnp
is mentioned by
dbSNPrs199774535
ebirs199774535
HLIrs199774535
Exacrs199774535
Varsomers199774535
Maprs199774535
PheGenIrs199774535
hapmaprs199774535
1000 genomesrs199774535
hgdprs199774535
ensemblrs199774535
gopubmedrs199774535
geneviewrs199774535
scholarrs199774535
googlers199774535
pharmgkbrs199774535
gwascentralrs199774535
openSNPrs199774535
23andMers199774535
23andMe allrs199774535
SNP Nexus

SNPshotrs199774535
SNPdbers199774535
MSV3drs199774535
GWAS Ctlgrs199774535
Max Magnitude0
ClinVar
Risk rs199774535(A,C;A,C)
Alt rs199774535(A,C;A,C)
Reference rs199774535(G;G)
Significance Pathogenic
Disease Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy Duchenne muscular dystrophy Dilated cardiomyopathy 3B
Reversed 0
HGVS NC_000023.10:g.32366608G>C
CLNSRC
CLNACC RCV000152879.3, RCV000152880.3, RCV000152881.3,