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rs863225088

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225088(C;G)
Make rs863225088(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position119100321
GeneDPAGT1
is asnp
is mentioned by
dbSNPrs863225088
ebirs863225088
HLIrs863225088
Exacrs863225088
Varsomers863225088
Maprs863225088
PheGenIrs863225088
hapmaprs863225088
1000 genomesrs863225088
hgdprs863225088
ensemblrs863225088
gopubmedrs863225088
geneviewrs863225088
scholarrs863225088
googlers863225088
pharmgkbrs863225088
gwascentralrs863225088
openSNPrs863225088
23andMers863225088
23andMe allrs863225088
SNP Nexus

SNPshotrs863225088
SNPdbers863225088
MSV3drs863225088
GWAS Ctlgrs863225088
Max Magnitude0
ClinVar
Risk rs863225088(G;G)
Alt rs863225088(G;G)
Reference rs863225088(C;C)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1J
Variation info
Gene DPAGT1
CLNDBN Congenital disorder of glycosylation type 1J
Reversed 1
HGVS NC_000011.9:g.118971031G>C
CLNSRC
CLNACC RCV000202322.1,