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rs1860190

From SNPedia

Orientationminus
Stabilizedminus
Make rs1860190(A;A)
Make rs1860190(A;T)
Make rs1860190(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position34249554
is asnp
is mentioned by
dbSNPrs1860190
ebirs1860190
HLIrs1860190
Exacrs1860190
Varsomers1860190
Maprs1860190
PheGenIrs1860190
hapmaprs1860190
1000 genomesrs1860190
hgdprs1860190
ensemblrs1860190
gopubmedrs1860190
geneviewrs1860190
scholarrs1860190
googlers1860190
pharmgkbrs1860190
gwascentralrs1860190
openSNPrs1860190
23andMers1860190
23andMe allrs1860190
SNP Nexus

SNPshotrs1860190
SNPdbers1860190
MSV3drs1860190
GWAS Ctlgrs1860190
GMAF0.4513
Max Magnitude
? (A;A) (A;T) (T;T) 28

[PMID 22117412] [Association of polymorphic markers of CCL2 gene with essential hypertension]

[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