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rs863225089

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225089(A;A)
Make rs863225089(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position74464919
GeneMOGS
is asnp
is mentioned by
dbSNPrs863225089
ebirs863225089
HLIrs863225089
Exacrs863225089
Varsomers863225089
Maprs863225089
PheGenIrs863225089
hapmaprs863225089
1000 genomesrs863225089
hgdprs863225089
ensemblrs863225089
gopubmedrs863225089
geneviewrs863225089
scholarrs863225089
googlers863225089
pharmgkbrs863225089
gwascentralrs863225089
openSNPrs863225089
23andMers863225089
23andMe allrs863225089
SNP Nexus

SNPshotrs863225089
SNPdbers863225089
MSV3drs863225089
GWAS Ctlgrs863225089
Max Magnitude0
ClinVar
Risk rs863225089(A;A)
Alt rs863225089(A;A)
Reference rs863225089(G;G)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 2B
Variation info
Gene MOGS
CLNDBN Congenital disorder of glycosylation type 2B
Reversed 1
HGVS NC_000002.11:g.74692046C>T
CLNSRC
CLNACC RCV000114957.4, RCV000201602.1,