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rs1546766

From SNPedia

Orientationminus
Stabilizedminus
Make rs1546766(A;A)
Make rs1546766(A;T)
Make rs1546766(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position79791769
is asnp
is mentioned by
dbSNPrs1546766
ebirs1546766
HLIrs1546766
Exacrs1546766
Varsomers1546766
Maprs1546766
PheGenIrs1546766
hapmaprs1546766
1000 genomesrs1546766
hgdprs1546766
ensemblrs1546766
gopubmedrs1546766
geneviewrs1546766
scholarrs1546766
googlers1546766
pharmgkbrs1546766
gwascentralrs1546766
openSNPrs1546766
23andMers1546766
23andMe allrs1546766
SNP Nexus

SNPshotrs1546766
SNPdbers1546766
MSV3drs1546766
GWAS Ctlgrs1546766
GMAF0.4646
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 22258388] Association of NOS2 and potential effect of VEGF, IL6, CCL2 and IL1RN polymorphisms and haplotypes on susceptibility to GCA--a simultaneous study of 130 potentially functional SNPs in 14 candidate genes