rs796052407

Orientation

minus

Stabilized

minus

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

Make rs796052407(C;T)

Make rs796052407(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

1759569

Gene

CTSD

is a	snp
is	mentioned by
dbSNP	rs796052407
dbSNP (classic)	rs796052407
ClinGen	rs796052407
ebi	rs796052407
HLI	rs796052407
Exac	rs796052407
Gnomad	rs796052407
Varsome	rs796052407
LitVar	rs796052407
Map	rs796052407
PheGenI	rs796052407
Biobank	rs796052407
1000 genomes	rs796052407
hgdp	rs796052407
ensembl	rs796052407
geneview	rs796052407
scholar	rs796052407
google	rs796052407
pharmgkb	rs796052407
gwascentral	rs796052407
openSNP	rs796052407
23andMe	rs796052407
SNPshot	rs796052407
SNPdbe	rs796052407
MSV3d	rs796052407
GWAS Ctlg	rs796052407

Max Magnitude

0

ClinVar
Risk	rs796052407(T;T)
Alt	rs796052407(T;T)
Reference	Rs796052407(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	CTSD
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.1780799G>A
CLNSRC
CLNACC	RCV000187320.1,