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rs587776747

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776747(C;C)
Make rs587776747(C;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position31261301
GeneDMD
is asnp
is mentioned by
dbSNPrs587776747
ebirs587776747
HLIrs587776747
Exacrs587776747
Varsomers587776747
Maprs587776747
PheGenIrs587776747
hapmaprs587776747
1000 genomesrs587776747
hgdprs587776747
ensemblrs587776747
gopubmedrs587776747
geneviewrs587776747
scholarrs587776747
googlers587776747
pharmgkbrs587776747
gwascentralrs587776747
openSNPrs587776747
23andMers587776747
23andMe allrs587776747
SNP Nexus

SNPshotrs587776747
SNPdbers587776747
MSV3drs587776747
GWAS Ctlgrs587776747
Max Magnitude0
ClinVar
Risk rs587776747(C,T;C,T)
Alt rs587776747(C,T;C,T)
Reference rs587776747(A;A)
Significance Pathogenic
Disease Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.31279418T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012038.5,