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rs4151659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs4151659(A;G)
Make rs4151659(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31950687
GeneCFB
is asnp
is mentioned by
dbSNPrs4151659
ebirs4151659
HLIrs4151659
Exacrs4151659
Varsomers4151659
Maprs4151659
PheGenIrs4151659
hapmaprs4151659
1000 genomesrs4151659
hgdprs4151659
ensemblrs4151659
gopubmedrs4151659
geneviewrs4151659
scholarrs4151659
googlers4151659
pharmgkbrs4151659
gwascentralrs4151659
openSNPrs4151659
23andMers4151659
23andMe allrs4151659
SNP Nexus

SNPshotrs4151659
SNPdbers4151659
MSV3drs4151659
GWAS Ctlgrs4151659
GMAF0.01837
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20054343OA-icon.png] Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes


[PMID 18806293] Analysis of rare variants in the complement component 2 (C2) and factor B (BF) genes refine association for age-related macular degeneration (AMD).


[PMID 19143814OA-icon.png] Several loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1.


[PMID 19143815OA-icon.png] MHC fine mapping of human type 1 diabetes using the T1DGC data.


[PMID 19259132OA-icon.png] Multilocus analysis of age-related macular degeneration.


GET Evidence
CFB-K565E
aa_change Lys565Glu
aa_change_short K565E
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0234375
summary