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rs2284664

From SNPedia

Orientationminus
Stabilizedminus
Make rs2284664(A;A)
Make rs2284664(A;G)
Make rs2284664(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position196733395
GeneCFH
is asnp
is mentioned by
dbSNPrs2284664
ebirs2284664
HLIrs2284664
Exacrs2284664
Varsomers2284664
Maprs2284664
PheGenIrs2284664
hapmaprs2284664
1000 genomesrs2284664
hgdprs2284664
ensemblrs2284664
gopubmedrs2284664
geneviewrs2284664
scholarrs2284664
googlers2284664
pharmgkbrs2284664
gwascentralrs2284664
openSNPrs2284664
23andMers2284664
23andMe allrs2284664
SNP Nexus

SNPshotrs2284664
SNPdbers2284664
MSV3drs2284664
GWAS Ctlgrs2284664
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24365176] Common variants in the complement factor H gene confer genetic susceptibility to central serous chorioretinopathy


[PMID 26217379] Ancestry of the Timorese: age-related macular degeneration associated genotype and allele sharing among human populations from throughout the world


[PMID 26296146] PREVALENCE OF THE COMPLEMENT FACTOR H AND GSTM1 GENES POLYMORPHISMS IN PATIENTS WITH CENTRAL SEROUS CHORIORETINOPATHY