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rs2357982

From SNPedia

Orientationplus
Stabilizedplus
Make rs2357982(C;C)
Make rs2357982(C;G)
Make rs2357982(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position161029592
is asnp
is mentioned by
dbSNPrs2357982
ebirs2357982
HLIrs2357982
Exacrs2357982
Varsomers2357982
Maprs2357982
PheGenIrs2357982
hapmaprs2357982
1000 genomesrs2357982
hgdprs2357982
ensemblrs2357982
gopubmedrs2357982
geneviewrs2357982
scholarrs2357982
googlers2357982
pharmgkbrs2357982
gwascentralrs2357982
openSNPrs2357982
23andMers2357982
23andMe allrs2357982
SNP Nexus

SNPshotrs2357982
SNPdbers2357982
MSV3drs2357982
GWAS Ctlgrs2357982
GMAF0.3163
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23509613OA-icon.png]
Trait Presence of antiphospholipid antibodies
Title Genome-wide association study of antiphospholipid antibodies.
Risk Allele
P-val 3E-6
Odds Ratio 2.19 [NR]