Have questions? Visit https://www.reddit.com/r/SNPedia

rs1020388

From SNPedia

Orientationminus
Stabilizedminus
Make rs1020388(A;A)
Make rs1020388(A;C)
Make rs1020388(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position56264200
is asnp
is mentioned by
dbSNPrs1020388
ebirs1020388
HLIrs1020388
Exacrs1020388
Varsomers1020388
Maprs1020388
PheGenIrs1020388
hapmaprs1020388
1000 genomesrs1020388
hgdprs1020388
ensemblrs1020388
gopubmedrs1020388
geneviewrs1020388
scholarrs1020388
googlers1020388
pharmgkbrs1020388
gwascentralrs1020388
openSNPrs1020388
23andMers1020388
23andMe allrs1020388
SNP Nexus

SNPshotrs1020388
SNPdbers1020388
MSV3drs1020388
GWAS Ctlgrs1020388
GMAF0.2479
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21383967OA-icon.png]
Trait
Title Meta-Analysis of Genome-Wide Association Studies in Celiac Disease and Rheumatoid Arthritis Identifies Fourteen Non-HLA Shared Loci
Risk Allele
P-val 3E-7
Odds Ratio None None