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rs373804251

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs373804251(A;G)
Make rs373804251(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32310127
GeneDMD
is asnp
is mentioned by
dbSNPrs373804251
ebirs373804251
HLIrs373804251
Exacrs373804251
Varsomers373804251
Maprs373804251
PheGenIrs373804251
hapmaprs373804251
1000 genomesrs373804251
hgdprs373804251
ensemblrs373804251
gopubmedrs373804251
geneviewrs373804251
scholarrs373804251
googlers373804251
pharmgkbrs373804251
gwascentralrs373804251
openSNPrs373804251
23andMers373804251
23andMe allrs373804251
SNP Nexus

SNPshotrs373804251
SNPdbers373804251
MSV3drs373804251
GWAS Ctlgrs373804251
Max Magnitude0
ClinVar
Risk rs373804251(G,T;G,T)
Alt rs373804251(G,T;G,T)
Reference rs373804251(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 0
HGVS NC_000023.10:g.32328244A>T
CLNSRC HGMD
CLNACC RCV000080682.4, RCV000178499.1, RCV000178500.1,