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rs702966

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs702966(C;C)
Make rs702966(C;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position611919
GenePHRF1
is asnp
is mentioned by
dbSNPrs702966
dbSNP (classic)rs702966
ClinGenrs702966
ebirs702966
HLIrs702966
Exacrs702966
Gnomadrs702966
Varsomers702966
LitVarrs702966
Maprs702966
PheGenIrs702966
Biobankrs702966
1000 genomesrs702966
hgdprs702966
ensemblrs702966
geneviewrs702966
scholarrs702966
googlers702966
pharmgkbrs702966
gwascentralrs702966
openSNPrs702966
23andMers702966
SNPshotrs702966
SNPdbers702966
MSV3drs702966
GWAS Ctlgrs702966
GMAF0.2787
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 20112359OA-icon.png] Genetic variation at the IRF7/PHRF1 locus is associated with autoantibody profile and serum interferon-alpha activity in lupus patients

[PMID 21167895] Association of genetic variations in the STAT4 and IRF7/KIAA1542 regions with systemic lupus erythematosus in a Northern Han Chinese population.

[PMID 21424379OA-icon.png] The role of polymorphisms in Toll-like receptors and their associated intracellular signaling genes in measles vaccine immunity.

[PMID 21926187OA-icon.png] Novel identification of the IRF7 region as an anticentromere autoantibody propensity locus in systemic sclerosis.