rs779703983

Orientation

plus

Stabilized

plus

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

Make rs779703983(G;G)

Make rs779703983(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

80217046

Gene

SGSH

is a	snp
is	mentioned by
dbSNP	rs779703983
dbSNP (classic)	rs779703983
ClinGen	rs779703983
ebi	rs779703983
HLI	rs779703983
Exac	rs779703983
Gnomad	rs779703983
Varsome	rs779703983
LitVar	rs779703983
Map	rs779703983
PheGenI	rs779703983
Biobank	rs779703983
1000 genomes	rs779703983
hgdp	rs779703983
ensembl	rs779703983
geneview	rs779703983
scholar	rs779703983
google	rs779703983
pharmgkb	rs779703983
gwascentral	rs779703983
openSNP	rs779703983
23andMe	rs779703983
SNPshot	rs779703983
SNPdbe	rs779703983
MSV3d	rs779703983
GWAS Ctlg	rs779703983

Max Magnitude

0

ClinVar
Risk	rs779703983(G;G)
Alt	rs779703983(G;G)
Reference	Rs779703983(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SGSH
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.78190845T>G
CLNSRC
CLNACC	RCV000413476.1,