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rs17791782

From SNPedia

Orientationplus
Stabilizedplus
Make rs17791782(A;A)
Make rs17791782(A;T)
Make rs17791782(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position17585424
GeneDSTN
is asnp
is mentioned by
dbSNPrs17791782
ebirs17791782
HLIrs17791782
Exacrs17791782
Varsomers17791782
Maprs17791782
PheGenIrs17791782
hapmaprs17791782
1000 genomesrs17791782
hgdprs17791782
ensemblrs17791782
gopubmedrs17791782
geneviewrs17791782
scholarrs17791782
googlers17791782
pharmgkbrs17791782
gwascentralrs17791782
openSNPrs17791782
23andMers17791782
23andMe allrs17791782
SNP Nexus

SNPshotrs17791782
SNPdbers17791782
MSV3drs17791782
GWAS Ctlgrs17791782
GMAF0.04224
Max Magnitude
? (A;A) (A;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 6E-6
Odds Ratio 2.63 [NR]