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rs16861990

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs16861990(A;C)
Make rs16861990(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position169165889
GeneNME7
is asnp
is mentioned by
dbSNPrs16861990
ebirs16861990
HLIrs16861990
Exacrs16861990
Varsomers16861990
Maprs16861990
PheGenIrs16861990
hapmaprs16861990
1000 genomesrs16861990
hgdprs16861990
ensemblrs16861990
gopubmedrs16861990
geneviewrs16861990
scholarrs16861990
googlers16861990
pharmgkbrs16861990
gwascentralrs16861990
openSNPrs16861990
23andMers16861990
23andMe allrs16861990
SNP Nexus

SNPshotrs16861990
SNPdbers16861990
MSV3drs16861990
GWAS Ctlgrs16861990
GMAF0.05005
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21502573OA-icon.png]
Trait
Title Genetic predictors of fibrin D-dimer levels in healthy adults.
Risk Allele C
P-val 0.000002
Odds Ratio 0.0614 [NR] % increase
GWAS snp
PMID [PMID 22672568OA-icon.png]
Trait
Title A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
Risk Allele C
P-val 2E-12
Odds Ratio 2.0200 None