rs28937886

Orientation

plus

Stabilized

plus

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

Make rs28937886(C;G)

Make rs28937886(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

45811163

Gene

SLC35C1

is a	snp
is	mentioned by
dbSNP	rs28937886
dbSNP (classic)	rs28937886
ClinGen	rs28937886
ebi	rs28937886
HLI	rs28937886
Exac	rs28937886
Gnomad	rs28937886
Varsome	rs28937886
LitVar	rs28937886
Map	rs28937886
PheGenI	rs28937886
Biobank	rs28937886
1000 genomes	rs28937886
hgdp	rs28937886
ensembl	rs28937886
geneview	rs28937886
scholar	rs28937886
google	rs28937886
pharmgkb	rs28937886
gwascentral	rs28937886
openSNP	rs28937886
23andMe	rs28937886
SNPshot	rs28937886
SNPdbe	rs28937886
MSV3d	rs28937886
GWAS Ctlg	rs28937886

Max Magnitude

0

OMIM	605881
Desc	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc
Variant	0002
Related	also

ClinVar
Risk	rs28937886(G;G)
Alt	rs28937886(G;G)
Reference	Rs28937886(C;C)
Significance	Pathogenic
Disease	Congenital disorder of glycosylation type 2C
Variation	info
Gene	SLC35C1
CLNDBN	Congenital disorder of glycosylation type 2C
Reversed	0
HGVS	NC_000011.9:g.45832714C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005006.3,