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rs17207494

From SNPedia

Orientationplus
Stabilizedplus
Make rs17207494(A;A)
Make rs17207494(A;C)
Make rs17207494(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position113106433
is asnp
is mentioned by
dbSNPrs17207494
ebirs17207494
HLIrs17207494
Exacrs17207494
Varsomers17207494
Maprs17207494
PheGenIrs17207494
hapmaprs17207494
1000 genomesrs17207494
hgdprs17207494
ensemblrs17207494
gopubmedrs17207494
geneviewrs17207494
scholarrs17207494
googlers17207494
pharmgkbrs17207494
gwascentralrs17207494
openSNPrs17207494
23andMers17207494
23andMe allrs17207494
SNP Nexus

SNPshotrs17207494
SNPdbers17207494
MSV3drs17207494
GWAS Ctlgrs17207494
GMAF0.2498
Max Magnitude
? (A;A) (A;C) (C;C) 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