rs10932037

Orientation

plus

Stabilized

plus

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

Make rs10932037(C;T)

Make rs10932037(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

203960623

Gene

ICOS

is a	snp
is	mentioned by
dbSNP	rs10932037
dbSNP (classic)	rs10932037
ClinGen	rs10932037
ebi	rs10932037
HLI	rs10932037
Exac	rs10932037
Gnomad	rs10932037
Varsome	rs10932037
LitVar	rs10932037
Map	rs10932037
PheGenI	rs10932037
Biobank	rs10932037
1000 genomes	rs10932037
hgdp	rs10932037
ensembl	rs10932037
geneview	rs10932037
scholar	rs10932037
google	rs10932037
pharmgkb	rs10932037
gwascentral	rs10932037
openSNP	rs10932037
23andMe	rs10932037
SNPshot	rs10932037
SNPdbe	rs10932037
MSV3d	rs10932037
GWAS Ctlg	rs10932037

GMAF

0.07025

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 19175525] CTLA4 and generalized vitiligo: two genetic association studies and a meta-analysis of published data

[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 18200060] PTPN22 is genetically associated with risk of generalized vitiligo, but CTLA4 is not.

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

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

ClinVar
Risk	rs10932037(T;T)
Alt	rs10932037(T;T)
Reference	Rs10932037(C;C)
Significance	Probable-non-pathogenic
Disease	Common Variable Immune Deficiency
Variation	info
Gene	ICOS
CLNDBN	Common Variable Immune Deficiency, Recessive
Reversed	0
HGVS	NC_000002.11:g.204825346C>T
CLNSRC
CLNACC	RCV000325562.1,