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rs727503830

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503830(A;T)
Make rs727503830(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32380549
GeneDMD
is asnp
is mentioned by
dbSNPrs727503830
ebirs727503830
HLIrs727503830
Exacrs727503830
Varsomers727503830
Maprs727503830
PheGenIrs727503830
hapmaprs727503830
1000 genomesrs727503830
hgdprs727503830
ensemblrs727503830
gopubmedrs727503830
geneviewrs727503830
scholarrs727503830
googlers727503830
pharmgkbrs727503830
gwascentralrs727503830
openSNPrs727503830
23andMers727503830
23andMe allrs727503830
SNP Nexus

SNPshotrs727503830
SNPdbers727503830
MSV3drs727503830
GWAS Ctlgrs727503830
Max Magnitude0
ClinVar
Risk rs727503830(T;T)
Alt rs727503830(T;T)
Reference rs727503830(A;A)
Significance Pathogenic
Disease not provided Duchenne muscular dystrophy Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN not provided Duchenne muscular dystrophy Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32398666T>A
CLNSRC
CLNACC RCV000152893.2, RCV000177781.1, RCV000177782.1,