rs587779410

Orientation

minus

Stabilized

minus

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

Make rs587779410(C;C)

Make rs587779410(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

6

Position

73641716

Gene

SLC17A5

is a	snp
is	mentioned by
dbSNP	rs587779410
dbSNP (classic)	rs587779410
ClinGen	rs587779410
ebi	rs587779410
HLI	rs587779410
Exac	rs587779410
Gnomad	rs587779410
Varsome	rs587779410
LitVar	rs587779410
Map	rs587779410
PheGenI	rs587779410
Biobank	rs587779410
1000 genomes	rs587779410
hgdp	rs587779410
ensembl	rs587779410
geneview	rs587779410
scholar	rs587779410
google	rs587779410
pharmgkb	rs587779410
gwascentral	rs587779410
openSNP	rs587779410
23andMe	rs587779410
SNPshot	rs587779410
SNPdbe	rs587779410
MSV3d	rs587779410
GWAS Ctlg	rs587779410

Max Magnitude

0

ClinVar
Risk	rs587779410(C;C)
Alt	rs587779410(C;C)
Reference	Rs587779410(T;T)
Significance	Pathogenic
Disease	Sialic acid storage disease
Variation	info
Gene	SLC17A5
CLNDBN	Sialic acid storage disease, severe infantile type
Reversed	1
HGVS	NC_000006.11:g.74351439A>G
CLNSRC
CLNACC	RCV000087101.1,