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rs1559931

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1559931(A;A)
Make rs1559931(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position203961006
GeneICOS
is asnp
is mentioned by
dbSNPrs1559931
dbSNP (old)rs1559931
ClinGenrs1559931
ebirs1559931
HLIrs1559931
Exacrs1559931
Gnomadrs1559931
Varsomers1559931
Maprs1559931
PheGenIrs1559931
Biobankrs1559931
1000 genomesrs1559931
hgdprs1559931
ensemblrs1559931
gopubmedrs1559931
geneviewrs1559931
scholarrs1559931
googlers1559931
pharmgkbrs1559931
gwascentralrs1559931
openSNPrs1559931
23andMers1559931
23andMe allrs1559931
SNP Nexus

SNPshotrs1559931
SNPdbers1559931
MSV3drs1559931
GWAS Ctlgrs1559931
GMAF0.2617
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 22977635OA-icon.png] 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,