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rs9315762

From SNPedia

Orientationplus
Stabilizedplus
Make rs9315762(C;C)
Make rs9315762(C;T)
Make rs9315762(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position40167770
is asnp
is mentioned by
dbSNPrs9315762
ebirs9315762
HLIrs9315762
Exacrs9315762
Varsomers9315762
Maprs9315762
PheGenIrs9315762
hapmaprs9315762
1000 genomesrs9315762
hgdprs9315762
ensemblrs9315762
gopubmedrs9315762
geneviewrs9315762
scholarrs9315762
googlers9315762
pharmgkbrs9315762
gwascentralrs9315762
openSNPrs9315762
23andMers9315762
23andMe allrs9315762
SNP Nexus

SNPshotrs9315762
SNPdbers9315762
MSV3drs9315762
GWAS Ctlgrs9315762
GMAF0.1928
Max Magnitude
? (C;C) (C;T) (T;T) 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 7E-6
Odds Ratio 2.26 [NR]


[PMID 18401594OA-icon.png] Genome-wide screen for asthma in Puerto Ricans: evidence for association with 5q23 region.