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rs863225086

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225086(A;G)
Make rs863225086(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position74897663
GeneMPI
is asnp
is mentioned by
dbSNPrs863225086
ebirs863225086
HLIrs863225086
Exacrs863225086
Varsomers863225086
Maprs863225086
PheGenIrs863225086
hapmaprs863225086
1000 genomesrs863225086
hgdprs863225086
ensemblrs863225086
gopubmedrs863225086
geneviewrs863225086
scholarrs863225086
googlers863225086
pharmgkbrs863225086
gwascentralrs863225086
openSNPrs863225086
23andMers863225086
23andMe allrs863225086
SNP Nexus

SNPshotrs863225086
SNPdbers863225086
MSV3drs863225086
GWAS Ctlgrs863225086
Max Magnitude0
ClinVar
Risk rs863225086(G;G)
Alt rs863225086(G;G)
Reference rs863225086(A;A)
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.75190004A>G
CLNSRC
CLNACC RCV000202323.1,