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rs6852535

From SNPedia

Orientationplus
Stabilizedplus
Make rs6852535(A;A)
Make rs6852535(A;G)
Make rs6852535(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position122557561
is asnp
is mentioned by
dbSNPrs6852535
ebirs6852535
HLIrs6852535
Exacrs6852535
Varsomers6852535
Maprs6852535
PheGenIrs6852535
hapmaprs6852535
1000 genomesrs6852535
hgdprs6852535
ensemblrs6852535
gopubmedrs6852535
geneviewrs6852535
scholarrs6852535
googlers6852535
pharmgkbrs6852535
gwascentralrs6852535
openSNPrs6852535
23andMers6852535
23andMe allrs6852535
SNP Nexus

SNPshotrs6852535
SNPdbers6852535
MSV3drs6852535
GWAS Ctlgrs6852535
GMAF0.247
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21685912OA-icon.png]
Trait
Title Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Risk Allele
P-val 1E-7
Odds Ratio 1.2300 [1.13-1.32]


[PMID 17558408OA-icon.png] A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.


[PMID 25037274] Autoimmune diseases association study with the KIAA1109-IL2-IL21 region in a Tunisian population