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rs398123932

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123932(-;-)
Make rs398123932(-;TTTCTAAAAA)
Make rs398123932(TTTCTAAAAA;TTTCTAAAAA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32464615
GeneDMD
is asnp
is mentioned by
dbSNPrs398123932
ebirs398123932
HLIrs398123932
Exacrs398123932
Varsomers398123932
Maprs398123932
PheGenIrs398123932
hapmaprs398123932
1000 genomesrs398123932
hgdprs398123932
ensemblrs398123932
gopubmedrs398123932
geneviewrs398123932
scholarrs398123932
googlers398123932
pharmgkbrs398123932
gwascentralrs398123932
openSNPrs398123932
23andMers398123932
23andMe allrs398123932
SNP Nexus

SNPshotrs398123932
SNPdbers398123932
MSV3drs398123932
GWAS Ctlgrs398123932
Max Magnitude0
ClinVar
Risk rs398123932(TTTCTAAAAA;TTTCTAAAAA)
Alt rs398123932(TTTCTAAAAA;TTTCTAAAAA)
Reference rs398123932(;)
Significance Pathogenic
Disease Dilated cardiomyopathy 3B
Variation info
Gene DMD
CLNDBN Dilated cardiomyopathy 3B
Reversed 1
HGVS NC_000023.10:g.32482732_32482733insTTTTTAGAAA
CLNSRC ClinVar
CLNACC RCV000080569.3,