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

rs6771725

From SNPedia

Orientationplus
Stabilizedplus
Make rs6771725(G;G)
Make rs6771725(G;T)
Make rs6771725(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position175357320
GeneNAALADL2
is asnp
is mentioned by
dbSNPrs6771725
ebirs6771725
HLIrs6771725
Exacrs6771725
Varsomers6771725
Maprs6771725
PheGenIrs6771725
hapmaprs6771725
1000 genomesrs6771725
hgdprs6771725
ensemblrs6771725
gopubmedrs6771725
geneviewrs6771725
scholarrs6771725
googlers6771725
pharmgkbrs6771725
gwascentralrs6771725
openSNPrs6771725
23andMers6771725
23andMe allrs6771725
SNP Nexus

SNPshotrs6771725
SNPdbers6771725
MSV3drs6771725
GWAS Ctlgrs6771725
GMAF0.3223
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 23509962OA-icon.png]
Trait Venous thromboembolism (gene x gene interaction)
Title A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
Risk Allele T
P-val 9E-9
Odds Ratio 2.22 [NR]