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rs72468700

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72468700(A;G)
Make rs72468700(G;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position32614462
GeneDMD
is asnp
is mentioned by
dbSNPrs72468700
ebirs72468700
HLIrs72468700
Exacrs72468700
Varsomers72468700
Maprs72468700
PheGenIrs72468700
hapmaprs72468700
1000 genomesrs72468700
hgdprs72468700
ensemblrs72468700
gopubmedrs72468700
geneviewrs72468700
scholarrs72468700
googlers72468700
pharmgkbrs72468700
gwascentralrs72468700
openSNPrs72468700
23andMers72468700
23andMe allrs72468700
SNP Nexus

SNPshotrs72468700
SNPdbers72468700
MSV3drs72468700
GWAS Ctlgrs72468700
Max Magnitude0
ClinVar
Risk rs72468700(C,G;C,G)
Alt rs72468700(C,G;C,G)
Reference rs72468700(A;A)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B Becker muscular dystrophy Duchenne muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32632579T>C
CLNSRC HGMD
CLNACC RCV000080445.4, RCV000174322.1, RCV000174323.1,