rs1064794815

Orientation

minus

Stabilized

minus

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

Chromosome

17

Position

80210766

Gene

SGSH

is a	snp
is	mentioned by
dbSNP	rs1064794815
dbSNP (classic)	rs1064794815
ClinGen	rs1064794815
ebi	rs1064794815
HLI	rs1064794815
Exac	rs1064794815
Gnomad	rs1064794815
Varsome	rs1064794815
LitVar	rs1064794815
Map	rs1064794815
PheGenI	rs1064794815
Biobank	rs1064794815
1000 genomes	rs1064794815
hgdp	rs1064794815
ensembl	rs1064794815
geneview	rs1064794815
scholar	rs1064794815
google	rs1064794815
pharmgkb	rs1064794815
gwascentral	rs1064794815
openSNP	rs1064794815
23andMe	rs1064794815
SNPshot	rs1064794815
SNPdbe	rs1064794815
MSV3d	rs1064794815
GWAS Ctlg	rs1064794815

Max Magnitude

0

ClinVar
Risk	rs1064794815(A;A)
Alt	rs1064794815(A;A)
Reference	Rs1064794815(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SGSH
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.78184565C>T
CLNSRC
CLNACC	RCV000478188.1,