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rs1290349

From SNPedia

Orientationplus
Stabilizedplus
Make rs1290349(A;A)
Make rs1290349(A;C)
Make rs1290349(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position112166831
GeneTEX12
is asnp
is mentioned by
dbSNPrs1290349
ebirs1290349
HLIrs1290349
Exacrs1290349
Varsomers1290349
Maprs1290349
PheGenIrs1290349
hapmaprs1290349
1000 genomesrs1290349
hgdprs1290349
ensemblrs1290349
gopubmedrs1290349
geneviewrs1290349
scholarrs1290349
googlers1290349
pharmgkbrs1290349
gwascentralrs1290349
openSNPrs1290349
23andMers1290349
23andMe allrs1290349
SNP Nexus

SNPshotrs1290349
SNPdbers1290349
MSV3drs1290349
GWAS Ctlgrs1290349
GMAF0.2287
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 22837141] Joint analysis of SNPs and proteins identifies regulatory IL18 gene variations decreasing the chance of spastic cerebral palsy