rs587777436

Orientation

plus

Stabilized

minus

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

Make rs587777436(A;A)

Make rs587777436(A;G)

Reference

GRCh38 38.1/142

Chromosome

X

Position

48905271

Gene

SLC35A2

is a	snp
is	mentioned by
dbSNP	rs587777436
dbSNP (classic)	rs587777436
ClinGen	rs587777436
ebi	rs587777436
HLI	rs587777436
Exac	rs587777436
Gnomad	rs587777436
Varsome	rs587777436
LitVar	rs587777436
Map	rs587777436
PheGenI	rs587777436
Biobank	rs587777436
1000 genomes	rs587777436
hgdp	rs587777436
ensembl	rs587777436
geneview	rs587777436
scholar	rs587777436
google	rs587777436
pharmgkb	rs587777436
gwascentral	rs587777436
openSNP	rs587777436
23andMe	rs587777436
SNPshot	rs587777436
SNPdbe	rs587777436
MSV3d	rs587777436
GWAS Ctlg	rs587777436

Max Magnitude

0

ClinVar
Risk	rs587777436(A;A) Rs587777436(G;G)
Alt	rs587777436(A;A) Rs587777436(G;G)
Reference	Rs587777436(C;C)
Significance	Pathogenic
Disease	CONGENITAL DISORDER OF GLYCOSYLATION
Variation	info
Gene	SLC35A2
CLNDBN	CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm
Reversed	1
HGVS	NC_000023.10:g.48762548G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000122746.3,