rs10183087

Orientation

plus

Stabilized

plus

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

Make rs10183087(A;C)

Make rs10183087(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

203959601

Gene

ICOS

is a	snp
is	mentioned by
dbSNP	rs10183087
dbSNP (classic)	rs10183087
ClinGen	rs10183087
ebi	rs10183087
HLI	rs10183087
Exac	rs10183087
Gnomad	rs10183087
Varsome	rs10183087
LitVar	rs10183087
Map	rs10183087
PheGenI	rs10183087
Biobank	rs10183087
1000 genomes	rs10183087
hgdp	rs10183087
ensembl	rs10183087
geneview	rs10183087
scholar	rs10183087
google	rs10183087
pharmgkb	rs10183087
gwascentral	rs10183087
openSNP	rs10183087
23andMe	rs10183087
SNPshot	rs10183087
SNPdbe	rs10183087
MSV3d	rs10183087
GWAS Ctlg	rs10183087

GMAF

0.2622

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

[PMID 21526489] ICOS gene polymorphisms in B-cell chronic lymphocytic leukemia in the Polish population

[PMID 21917182] ICOS gene polymorphisms are associated with sporadic breast cancer: a case-control study

[PMID 19202444] Association of genetic variation in inducible costimulator gene with outcome of kidney transplantation.

[PMID 19672595] Polymorphisms in the CD28/CTLA4/ICOS genes: role in malignant melanoma susceptibility and prognosis?

[PMID 19747393] Improving power in genetic-association studies via wavelet transformation.

[PMID 22977635] Association study between polymorphisms of CD28, CTLA4 and ICOS and non-segmental vitiligo in a Korean population

[PMID 24083358] Effect of Soluble Inducible Costimulator Level and Its Polymorphisms on Age-Related Macular Degeneration

ClinVar
Risk	rs10183087(C;C) rs10183087(G;G)
Alt	rs10183087(C;C) rs10183087(G;G)
Reference	Rs10183087(A;A)
Significance	Probable-non-pathogenic
Disease	Common Variable Immune Deficiency not specified
Variation	info
Gene	ICOS
CLNDBN	Common Variable Immune Deficiency, Recessive not specified
Reversed	0
HGVS	NC_000002.11:g.204824324A>C
CLNSRC
CLNACC	RCV000311000.1, RCV000454953.1,