rs28928906

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs28928906(A;A)

Make rs28928906(A;G)

Reference

GRCh38 38.1/142

Chromosome

15

Position

74897050

Gene

MPI

is a	snp
is	mentioned by
dbSNP	rs28928906
dbSNP (classic)	rs28928906
ClinGen	rs28928906
ebi	rs28928906
HLI	rs28928906
Exac	rs28928906
Gnomad	rs28928906
Varsome	rs28928906
LitVar	rs28928906
Map	rs28928906
PheGenI	rs28928906
Biobank	rs28928906
1000 genomes	rs28928906
hgdp	rs28928906
ensembl	rs28928906
geneview	rs28928906
scholar	rs28928906
google	rs28928906
pharmgkb	rs28928906
gwascentral	rs28928906
openSNP	rs28928906
23andMe	rs28928906
SNPshot	rs28928906
SNPdbe	rs28928906
MSV3d	rs28928906
GWAS Ctlg	rs28928906

Max Magnitude

0

OMIM	154550
Desc	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ib
Variant	0005
Related	also

ClinVar
Risk	rs28928906(A;A)
Alt	rs28928906(A;A)
Reference	Rs28928906(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.75189391G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015423.28,