rs796052400

Orientation

minus

Stabilized

minus

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

Make rs796052400(C;G)

Make rs796052400(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

1759606

Gene

CTSD

is a	snp
is	mentioned by
dbSNP	rs796052400
dbSNP (classic)	rs796052400
ClinGen	rs796052400
ebi	rs796052400
HLI	rs796052400
Exac	rs796052400
Gnomad	rs796052400
Varsome	rs796052400
LitVar	rs796052400
Map	rs796052400
PheGenI	rs796052400
Biobank	rs796052400
1000 genomes	rs796052400
hgdp	rs796052400
ensembl	rs796052400
geneview	rs796052400
scholar	rs796052400
google	rs796052400
pharmgkb	rs796052400
gwascentral	rs796052400
openSNP	rs796052400
23andMe	rs796052400
SNPshot	rs796052400
SNPdbe	rs796052400
MSV3d	rs796052400
GWAS Ctlg	rs796052400

Max Magnitude

0

ClinVar
Risk	rs796052400(G;G)
Alt	rs796052400(G;G)
Reference	Rs796052400(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CTSD
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.1780836G>C
CLNSRC
CLNACC	RCV000187307.1,