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rs387906831

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906831(A;A)
Make rs387906831(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position20654660
GeneDDOST
is asnp
is mentioned by
dbSNPrs387906831
ebirs387906831
HLIrs387906831
Exacrs387906831
Varsomers387906831
Maprs387906831
PheGenIrs387906831
hapmaprs387906831
1000 genomesrs387906831
hgdprs387906831
ensemblrs387906831
gopubmedrs387906831
geneviewrs387906831
scholarrs387906831
googlers387906831
pharmgkbrs387906831
gwascentralrs387906831
openSNPrs387906831
23andMers387906831
23andMe allrs387906831
SNP Nexus

SNPshotrs387906831
SNPdbers387906831
MSV3drs387906831
GWAS Ctlgrs387906831
Max Magnitude0
ClinVar
Risk rs387906831(A;A)
Alt rs387906831(A;A)
Reference rs387906831(G;G)
Significance Pathogenic
Disease Congenital order of glycosylation type 1r
Variation info
Gene DDOST
CLNDBN Congenital order of glycosylation type 1r
Reversed 1
HGVS NC_000001.10:g.20981153C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023170.5,