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rs863225087

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225087(A;A)
Make rs863225087(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position74897711
GeneMPI
is asnp
is mentioned by
dbSNPrs863225087
ebirs863225087
HLIrs863225087
Exacrs863225087
Varsomers863225087
Maprs863225087
PheGenIrs863225087
hapmaprs863225087
1000 genomesrs863225087
hgdprs863225087
ensemblrs863225087
gopubmedrs863225087
geneviewrs863225087
scholarrs863225087
googlers863225087
pharmgkbrs863225087
gwascentralrs863225087
openSNPrs863225087
23andMers863225087
23andMe allrs863225087
SNP Nexus

SNPshotrs863225087
SNPdbers863225087
MSV3drs863225087
GWAS Ctlgrs863225087
Max Magnitude0
ClinVar
Risk rs863225087(A;A)
Alt rs863225087(A;A)
Reference rs863225087(G;G)
Significance Pathogenic
Disease Congenital disorder of glycosylation type 1B
Variation info
Gene MPI
CLNDBN Congenital disorder of glycosylation type 1B
Reversed 0
HGVS NC_000015.9:g.75190052G>A
CLNSRC
CLNACC RCV000202324.1,