rs1057517115

Orientation

plus

Stabilized

plus

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

Make rs1057517115(-;-)

Make rs1057517115(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

74896221

Gene

MPI

is a	snp
is	mentioned by
dbSNP	rs1057517115
dbSNP (classic)	rs1057517115
ClinGen	rs1057517115
ebi	rs1057517115
HLI	rs1057517115
Exac	rs1057517115
Gnomad	rs1057517115
Varsome	rs1057517115
LitVar	rs1057517115
Map	rs1057517115
PheGenI	rs1057517115
Biobank	rs1057517115
1000 genomes	rs1057517115
hgdp	rs1057517115
ensembl	rs1057517115
geneview	rs1057517115
scholar	rs1057517115
google	rs1057517115
pharmgkb	rs1057517115
gwascentral	rs1057517115
openSNP	rs1057517115
23andMe	rs1057517115
SNPshot	rs1057517115
SNPdbe	rs1057517115
MSV3d	rs1057517115
GWAS Ctlg	rs1057517115

Max Magnitude

0

ClinVar
Risk	rs1057517115(-;-)
Alt	rs1057517115(-;-)
Reference	Rs1057517115(G;G)
Significance	Probable-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.75188562delG
CLNSRC
CLNACC	RCV000409548.1,