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rs398123960

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123960(A;A)
Make rs398123960(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32389496
GeneDMD
is asnp
is mentioned by
dbSNPrs398123960
ebirs398123960
HLIrs398123960
Exacrs398123960
Varsomers398123960
Maprs398123960
PheGenIrs398123960
hapmaprs398123960
1000 genomesrs398123960
hgdprs398123960
ensemblrs398123960
gopubmedrs398123960
geneviewrs398123960
scholarrs398123960
googlers398123960
pharmgkbrs398123960
gwascentralrs398123960
openSNPrs398123960
23andMers398123960
23andMe allrs398123960
SNP Nexus

SNPshotrs398123960
SNPdbers398123960
MSV3drs398123960
GWAS Ctlgrs398123960
Max Magnitude0
ClinVar
Risk rs398123960(A,C;A,C)
Alt rs398123960(A,C;A,C)
Reference rs398123960(G;G)
Significance Pathogenic
Disease not provided Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN not provided Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32407613C>G; NC_000023.10:g.32407613C>T
CLNSRC HGMD
CLNACC RCV000080621.4, RCV000080620.3,