rs1559931

plus

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

Make rs1559931(A;A)

Make rs1559931(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

203961006

Gene

ICOS

is a	snp
is	mentioned by
dbSNP	rs1559931
dbSNP (classic)	rs1559931
ClinGen	rs1559931
ebi	rs1559931
HLI	rs1559931
Exac	rs1559931
Gnomad	rs1559931
Varsome	rs1559931
LitVar	rs1559931
Map	rs1559931
PheGenI	rs1559931
Biobank	rs1559931
1000 genomes	rs1559931
hgdp	rs1559931
ensembl	rs1559931
geneview	rs1559931
scholar	rs1559931
google	rs1559931
pharmgkb	rs1559931
gwascentral	rs1559931
openSNP	rs1559931
23andMe	rs1559931
SNPshot	rs1559931
SNPdbe	rs1559931
MSV3d	rs1559931
GWAS Ctlg	rs1559931

GMAF

0.2617

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

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

[PMID 25497975] Five functional polymorphisms of B7/CD28 co-signaling molecules alter susceptibility to colorectal cancer

[PMID 26074057] Association of inducible T-cell costimulator polymorphisms with susceptibility and outcome of hepatitis B virus infection in a Chinese Han population

ClinVar
Risk	rs1559931(A;A)
Alt	rs1559931(A;A)
Reference	Rs1559931(G;G)
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.204825729G>A
CLNSRC
CLNACC	RCV000298214.1,

[PMID 30600290] The Effect of ICOS Polymorphism Interactions with HBV Mutations on HBV Subtype Infection Outcomes.