rs587779409

Orientation

minus

Stabilized

minus

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

Make rs587779409(C;T)

Make rs587779409(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

1758970

Gene

CTSD

is a	snp
is	mentioned by
dbSNP	rs587779409
dbSNP (classic)	rs587779409
ClinGen	rs587779409
ebi	rs587779409
HLI	rs587779409
Exac	rs587779409
Gnomad	rs587779409
Varsome	rs587779409
LitVar	rs587779409
Map	rs587779409
PheGenI	rs587779409
Biobank	rs587779409
1000 genomes	rs587779409
hgdp	rs587779409
ensembl	rs587779409
geneview	rs587779409
scholar	rs587779409
google	rs587779409
pharmgkb	rs587779409
gwascentral	rs587779409
openSNP	rs587779409
23andMe	rs587779409
SNPshot	rs587779409
SNPdbe	rs587779409
MSV3d	rs587779409
GWAS Ctlg	rs587779409

Max Magnitude

0

ClinVar
Risk	rs587779409(T;T)
Alt	rs587779409(T;T)
Reference	Rs587779409(C;C)
Significance	Pathogenic
Disease	Ceroid lipofuscinosis neuronal 10
Variation	info
Gene	CTSD
CLNDBN	Ceroid lipofuscinosis neuronal 10
Reversed	1
HGVS	NC_000011.9:g.1780200G>A
CLNSRC
CLNACC	RCV000087098.1,