rs587776961

Orientation

plus

Stabilized

minus

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

Make rs587776961(C;T)

Make rs587776961(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

48904918

Gene

SLC35A2

is a	snp
is	mentioned by
dbSNP	rs587776961
dbSNP (classic)	rs587776961
ClinGen	rs587776961
ebi	rs587776961
HLI	rs587776961
Exac	rs587776961
Gnomad	rs587776961
Varsome	rs587776961
LitVar	rs587776961
Map	rs587776961
PheGenI	rs587776961
Biobank	rs587776961
1000 genomes	rs587776961
hgdp	rs587776961
ensembl	rs587776961
geneview	rs587776961
scholar	rs587776961
google	rs587776961
pharmgkb	rs587776961
gwascentral	rs587776961
openSNP	rs587776961
23andMe	rs587776961
SNPshot	rs587776961
SNPdbe	rs587776961
MSV3d	rs587776961
GWAS Ctlg	rs587776961

Max Magnitude

0

ClinVar
Risk	Rs587776961(C;C) rs587776961(T;T)
Alt	Rs587776961(C;C) rs587776961(T;T)
Reference	Rs587776961(G;G)
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.48762195C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000043515.8,