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rs121909291

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909291(C;C)
Make rs121909291(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position74462332
GeneMOGS
is asnp
is mentioned by
dbSNPrs121909291
ebirs121909291
HLIrs121909291
Exacrs121909291
Varsomers121909291
Maprs121909291
PheGenIrs121909291
hapmaprs121909291
1000 genomesrs121909291
hgdprs121909291
ensemblrs121909291
gopubmedrs121909291
geneviewrs121909291
scholarrs121909291
googlers121909291
pharmgkbrs121909291
gwascentralrs121909291
openSNPrs121909291
23andMers121909291
23andMe allrs121909291
SNP Nexus

SNPshotrs121909291
SNPdbers121909291
MSV3drs121909291
GWAS Ctlgrs121909291
Max Magnitude0
OMIM601336
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909291(A,C;A,C)
Alt rs121909291(A,C;A,C)
Reference rs121909291(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.74689459C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008676.3,