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rs2075726

From SNPedia

Orientationplus
Stabilizedplus
Make rs2075726(A;A)
Make rs2075726(A;G)
Make rs2075726(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position36914004
GeneCSF2RB
is asnp
is mentioned by
dbSNPrs2075726
dbSNP (classic)rs2075726
ClinGenrs2075726
ebirs2075726
HLIrs2075726
Exacrs2075726
Gnomadrs2075726
Varsomers2075726
LitVarrs2075726
Maprs2075726
PheGenIrs2075726
Biobankrs2075726
1000 genomesrs2075726
hgdprs2075726
ensemblrs2075726
geneviewrs2075726
scholarrs2075726
googlers2075726
pharmgkbrs2075726
gwascentralrs2075726
openSNPrs2075726
23andMers2075726
SNPshotrs2075726
SNPdbers2075726
MSV3drs2075726
GWAS Ctlgrs2075726
GMAF0.4288
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22138694]
Trait
Title A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis.
Risk Allele G
P-val 0.000009
Odds Ratio 1.1400 None