rs217086

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(G;G)	0	common on affy axiom data

Make rs217086(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

88312415

Gene

CTSC

is a	snp
is	mentioned by
dbSNP	rs217086
dbSNP (classic)	rs217086
ClinGen	rs217086
ebi	rs217086
HLI	rs217086
Exac	rs217086
Gnomad	rs217086
Varsome	rs217086
LitVar	rs217086
Map	rs217086
PheGenI	rs217086
Biobank	rs217086
1000 genomes	rs217086
hgdp	rs217086
ensembl	rs217086
geneview	rs217086
scholar	rs217086
google	rs217086
pharmgkb	rs217086
gwascentral	rs217086
openSNP	rs217086
23andMe	rs217086
SNPshot	rs217086
SNPdbe	rs217086
MSV3d	rs217086
GWAS Ctlg	rs217086

GMAF

0.08815

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	Rs217086(G;G)
Alt	Rs217086(G;G)
Reference	Rs217086(A;A)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	CTSC
CLNDBN	not specified
Reversed	0
HGVS	NC_000011.9:g.88045583A>G
CLNSRC
CLNACC	RCV000454700.1,