rs28937571

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(T;T)	0

Make rs28937571(A;G)

Make rs28937571(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

88294163

Gene

CTSC

is a	snp
is	mentioned by
dbSNP	rs28937571
dbSNP (classic)	rs28937571
ClinGen	rs28937571
ebi	rs28937571
HLI	rs28937571
Exac	rs28937571
Gnomad	rs28937571
Varsome	rs28937571
LitVar	rs28937571
Map	rs28937571
PheGenI	rs28937571
Biobank	rs28937571
1000 genomes	rs28937571
hgdp	rs28937571
ensembl	rs28937571
geneview	rs28937571
scholar	rs28937571
google	rs28937571
pharmgkb	rs28937571
gwascentral	rs28937571
openSNP	rs28937571
23andMe	rs28937571
SNPshot	rs28937571
SNPdbe	rs28937571
MSV3d	rs28937571
GWAS Ctlg	rs28937571

Max Magnitude

0

OMIM	602365
Desc	PERIODONTITIS, AGGRESSIVE, 1
Variant	0012
Related	also

ClinVar
Risk	rs28937571(G;G)
Alt	rs28937571(G;G)
Reference	Rs28937571(A;A)
Significance	Pathogenic
Disease	Periodontitis
Variation	info
Gene	CTSC
CLNDBN	Periodontitis, aggressive, 1
Reversed	1
HGVS	NC_000011.9:g.88027331T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007723.3,