rs28939087

Orientation

plus

Stabilized

plus

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

Make rs28939087(C;T)

Make rs28939087(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

45806240

Gene

SLC35C1

is a	snp
is	mentioned by
dbSNP	rs28939087
dbSNP (classic)	rs28939087
ClinGen	rs28939087
ebi	rs28939087
HLI	rs28939087
Exac	rs28939087
Gnomad	rs28939087
Varsome	rs28939087
LitVar	rs28939087
Map	rs28939087
PheGenI	rs28939087
Biobank	rs28939087
1000 genomes	rs28939087
hgdp	rs28939087
ensembl	rs28939087
geneview	rs28939087
scholar	rs28939087
google	rs28939087
pharmgkb	rs28939087
gwascentral	rs28939087
openSNP	rs28939087
23andMe	rs28939087
SNPshot	rs28939087
SNPdbe	rs28939087
MSV3d	rs28939087
GWAS Ctlg	rs28939087

Max Magnitude

0

OMIM	605881
Desc	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIc
Variant	0001
Related	also

ClinVar
Risk	rs28939087(T;T)
Alt	rs28939087(T;T)
Reference	Rs28939087(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.45827791C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005005.3,