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rs3753396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs3753396(A;G)
Make rs3753396(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position196726612
GeneCFH
is asnp
is mentioned by
dbSNPrs3753396
ebirs3753396
HLIrs3753396
Exacrs3753396
Varsomers3753396
Maprs3753396
PheGenIrs3753396
hapmaprs3753396
1000 genomesrs3753396
hgdprs3753396
ensemblrs3753396
gopubmedrs3753396
geneviewrs3753396
scholarrs3753396
googlers3753396
pharmgkbrs3753396
gwascentralrs3753396
openSNPrs3753396
23andMers3753396
23andMe allrs3753396
SNP Nexus

SNPshotrs3753396
SNPdbers3753396
MSV3drs3753396
GWAS Ctlgrs3753396
GMAF0.2337
Max Magnitude0
? (A;A) (A;G) (G;G) 28
age related macular degeneration [PMID 18421087]


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[PMID 18162041OA-icon.png] Neovascular age-related macular degeneration risk based on CFH, LOC387715/HTRA1, and smoking.

[PMID 18483746OA-icon.png] Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutation.

[PMID 19861685OA-icon.png] Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome.

[PMID 19958499OA-icon.png] A particle swarm based hybrid system for imbalanced medical data sampling.

[PMID 20157618OA-icon.png] Complement component 3: an assessment of association with AMD and analysis of gene-gene and gene-environment interactions in a Northern Irish cohort.


[PMID 25798599OA-icon.png] Susceptibility to Invasive Meningococcal Disease: Polymorphism of Complement System Genes and Neisseria meningitidis Factor H Binding Protein