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rs7574862

From SNPedia

Orientationplus
Stabilizedplus
Make rs7574862(A;A)
Make rs7574862(A;G)
Make rs7574862(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position95302457
GeneKCNIP3
is asnp
is mentioned by
dbSNPrs7574862
ebirs7574862
HLIrs7574862
Exacrs7574862
Varsomers7574862
Maprs7574862
PheGenIrs7574862
hapmaprs7574862
1000 genomesrs7574862
hgdprs7574862
ensemblrs7574862
gopubmedrs7574862
geneviewrs7574862
scholarrs7574862
googlers7574862
pharmgkbrs7574862
gwascentralrs7574862
openSNPrs7574862
23andMers7574862
23andMe allrs7574862
SNP Nexus

SNPshotrs7574862
SNPdbers7574862
MSV3drs7574862
GWAS Ctlgrs7574862
GMAF0.2723
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 22133489] The polymorphisms of T cell-specific TBX21 and STAT4 genes may contribute to the susceptibility of Chinese individuals to aplastic anemia