rs753666460

Orientation

plus

Stabilized

plus

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

Make rs753666460(C;T)

Make rs753666460(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

80214264

Gene

SGSH

is a	snp
is	mentioned by
dbSNP	rs753666460
dbSNP (classic)	rs753666460
ClinGen	rs753666460
ebi	rs753666460
HLI	rs753666460
Exac	rs753666460
Gnomad	rs753666460
Varsome	rs753666460
LitVar	rs753666460
Map	rs753666460
PheGenI	rs753666460
Biobank	rs753666460
1000 genomes	rs753666460
hgdp	rs753666460
ensembl	rs753666460
geneview	rs753666460
scholar	rs753666460
google	rs753666460
pharmgkb	rs753666460
gwascentral	rs753666460
openSNP	rs753666460
23andMe	rs753666460
SNPshot	rs753666460
SNPdbe	rs753666460
MSV3d	rs753666460
GWAS Ctlg	rs753666460

Max Magnitude

0

ClinVar
Risk	rs753666460(T;T)
Alt	rs753666460(T;T)
Reference	Rs753666460(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SGSH
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.78188063C>T
CLNSRC
CLNACC	RCV000413143.1,