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rs2838519

From SNPedia

Orientationplus
Stabilizedplus
Make rs2838519(A;A)
Make rs2838519(A;G)
Make rs2838519(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position44195140
GeneC21orf33
is asnp
is mentioned by
dbSNPrs2838519
ebirs2838519
HLIrs2838519
Exacrs2838519
Varsomers2838519
Maprs2838519
PheGenIrs2838519
hapmaprs2838519
1000 genomesrs2838519
hgdprs2838519
ensemblrs2838519
gopubmedrs2838519
geneviewrs2838519
scholarrs2838519
googlers2838519
pharmgkbrs2838519
gwascentralrs2838519
openSNPrs2838519
23andMers2838519
23andMe allrs2838519
SNP Nexus

SNPshotrs2838519
SNPdbers2838519
MSV3drs2838519
GWAS Ctlgrs2838519
GMAF0.4568
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21297633OA-icon.png]
Trait
Title Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47
Risk Allele G
P-val 6E-11
Odds Ratio 1.1400 [1.05-1.22]


[PMID 20217071OA-icon.png] Impact of female cigarette smoking on circulating B cells in vivo: the suppressed ICOSLG, TCF3, and VCAM1 gene functional network may inhibit normal cell function.

GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait Crohn's disease
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
Risk Allele G
P-val 2E-14
Odds Ratio 1.18 [1.13-1.23]


[PMID 24480412] PTPN2 rs1893217 single-nucleotide polymorphism is associated with risk of Behçet's disease in a Chinese Han population