rs763407972

Orientation

plus

Stabilized

plus

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

Make rs763407972(C;T)

Make rs763407972(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

1754982

Gene

CTSD

is a	snp
is	mentioned by
dbSNP	rs763407972
dbSNP (classic)	rs763407972
ClinGen	rs763407972
ebi	rs763407972
HLI	rs763407972
Exac	rs763407972
Gnomad	rs763407972
Varsome	rs763407972
LitVar	rs763407972
Map	rs763407972
PheGenI	rs763407972
Biobank	rs763407972
1000 genomes	rs763407972
hgdp	rs763407972
ensembl	rs763407972
geneview	rs763407972
scholar	rs763407972
google	rs763407972
pharmgkb	rs763407972
gwascentral	rs763407972
openSNP	rs763407972
23andMe	rs763407972
SNPshot	rs763407972
SNPdbe	rs763407972
MSV3d	rs763407972
GWAS Ctlg	rs763407972

Max Magnitude

0

ClinVar
Risk	rs763407972(T;T)
Alt	rs763407972(T;T)
Reference	Rs763407972(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	CTSD
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.1776212C>T
CLNSRC
CLNACC	RCV000187314.1,