Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123881

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAAAA;GAAAA) 0 common in clinvar
Make rs398123881(-;-)
Make rs398123881(-;GAAAA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32518015
GeneDMD
is asnp
is mentioned by
dbSNPrs398123881
ebirs398123881
HLIrs398123881
Exacrs398123881
Varsomers398123881
Maprs398123881
PheGenIrs398123881
hapmaprs398123881
1000 genomesrs398123881
hgdprs398123881
ensemblrs398123881
gopubmedrs398123881
geneviewrs398123881
scholarrs398123881
googlers398123881
pharmgkbrs398123881
gwascentralrs398123881
openSNPrs398123881
23andMers398123881
23andMe allrs398123881
SNP Nexus

SNPshotrs398123881
SNPdbers398123881
MSV3drs398123881
GWAS Ctlgrs398123881
Max Magnitude0
ClinVar
Risk rs398123881(;)
Alt rs398123881(;)
Reference rs398123881(GAAAA;GAAAA)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32536132_32536136delTTTTC
CLNSRC HGMD
CLNACC RCV000080487.3,