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rs398123978

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs398123978(ATGAATGAATTCATT;ATGAATGAATTCATT)
Make rs398123978(ATGAATGAATTCATT;CA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position32364638
GeneDMD
is asnp
is mentioned by
dbSNPrs398123978
ebirs398123978
HLIrs398123978
Exacrs398123978
Varsomers398123978
Maprs398123978
PheGenIrs398123978
hapmaprs398123978
1000 genomesrs398123978
hgdprs398123978
ensemblrs398123978
gopubmedrs398123978
geneviewrs398123978
scholarrs398123978
googlers398123978
pharmgkbrs398123978
gwascentralrs398123978
openSNPrs398123978
23andMers398123978
23andMe allrs398123978
SNP Nexus

SNPshotrs398123978
SNPdbers398123978
MSV3drs398123978
GWAS Ctlgrs398123978
Max Magnitude0
ClinVar
Risk rs398123978(ATGAATGAATTCATT;ATGAATGAATTCATT)
Alt rs398123978(ATGAATGAATTCATT;ATGAATGAATTCATT)
Reference rs398123978(CA;CA)
Significance Pathogenic
Disease not provided
Variation info
Gene DMD
CLNDBN not provided
Reversed 1
HGVS NC_000023.11:g.32364638_32364639delTGinsAATGAATTCATTCAT
CLNSRC ClinVar
CLNACC RCV000080642.1,