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rs398124001

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124001(G;T)
Make rs398124001(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32310261
GeneDMD
is asnp
is mentioned by
dbSNPrs398124001
ebirs398124001
HLIrs398124001
Exacrs398124001
Varsomers398124001
Maprs398124001
PheGenIrs398124001
hapmaprs398124001
1000 genomesrs398124001
hgdprs398124001
ensemblrs398124001
gopubmedrs398124001
geneviewrs398124001
scholarrs398124001
googlers398124001
pharmgkbrs398124001
gwascentralrs398124001
openSNPrs398124001
23andMers398124001
23andMe allrs398124001
SNP Nexus

SNPshotrs398124001
SNPdbers398124001
MSV3drs398124001
GWAS Ctlgrs398124001
Max Magnitude0
ClinVar
Risk rs398124001(T;T)
Alt rs398124001(T;T)
Reference rs398124001(G;G)
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.32328378C>A
CLNSRC HGMD
CLNACC RCV000080677.4, RCV000178495.1, RCV000178496.1,