rs587777534

Orientation

plus

Stabilized

plus

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

Make rs587777534(C;T)

Make rs587777534(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

88296207

Gene

CTSC

is a	snp
is	mentioned by
dbSNP	rs587777534
dbSNP (classic)	rs587777534
ClinGen	rs587777534
ebi	rs587777534
HLI	rs587777534
Exac	rs587777534
Gnomad	rs587777534
Varsome	rs587777534
LitVar	rs587777534
Map	rs587777534
PheGenI	rs587777534
Biobank	rs587777534
1000 genomes	rs587777534
hgdp	rs587777534
ensembl	rs587777534
geneview	rs587777534
scholar	rs587777534
google	rs587777534
pharmgkb	rs587777534
gwascentral	rs587777534
openSNP	rs587777534
23andMe	rs587777534
SNPshot	rs587777534
SNPdbe	rs587777534
MSV3d	rs587777534
GWAS Ctlg	rs587777534

Max Magnitude

0

ClinVar
Risk	rs587777534(G;G) rs587777534(T;T)
Alt	rs587777534(G;G) rs587777534(T;T)
Reference	Rs587777534(C;C)
Significance	Pathogenic
Disease	Periodontitis
Variation	info
Gene	CTSC
CLNDBN	Periodontitis, aggressive, 1
Reversed	0
HGVS	NC_000011.9:g.88029375C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000128620.3,