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rs2927488

From SNPedia

Orientationplus
Stabilizedplus
Make rs2927488(A;A)
Make rs2927488(A;G)
Make rs2927488(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44728212
is asnp
is mentioned by
dbSNPrs2927488
ebirs2927488
HLIrs2927488
Exacrs2927488
Varsomers2927488
Maprs2927488
PheGenIrs2927488
hapmaprs2927488
1000 genomesrs2927488
hgdprs2927488
ensemblrs2927488
gopubmedrs2927488
geneviewrs2927488
scholarrs2927488
googlers2927488
pharmgkbrs2927488
gwascentralrs2927488
openSNPrs2927488
23andMers2927488
23andMe allrs2927488
SNP Nexus

SNPshotrs2927488
SNPdbers2927488
MSV3drs2927488
GWAS Ctlgrs2927488
GMAF0.2231
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20601676] Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease


[PMID 21390209OA-icon.png] Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease.