rs2072633

Orientation

minus

Stabilized

minus

Make rs2072633(C;C)

Make rs2072633(C;T)

Make rs2072633(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31951801

Gene	CFB, NELFE

is a	snp
is	mentioned by
dbSNP	rs2072633
dbSNP (classic)	rs2072633
ClinGen	rs2072633
ebi	rs2072633
HLI	rs2072633
Exac	rs2072633
Gnomad	rs2072633
Varsome	rs2072633
LitVar	rs2072633
Map	rs2072633
PheGenI	rs2072633
Biobank	rs2072633
1000 genomes	rs2072633
hgdp	rs2072633
ensembl	rs2072633
geneview	rs2072633
scholar	rs2072633
google	rs2072633
pharmgkb	rs2072633
gwascentral	rs2072633
openSNP	rs2072633
23andMe	rs2072633
SNPshot	rs2072633
SNPdbe	rs2072633
MSV3d	rs2072633
GWAS Ctlg	rs2072633

GMAF

0.388

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 19654554 ] The Major Histocompatibility Complex Conserved Extended Haplotype 8.1 in AIDS-Related Non-Hodgkin Lymphoma

[PMID 17660530] Risk alleles for multiple sclerosis identified by a genomewide study.

[PMID 18493315 ] C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes.

[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 19259132 ] Multilocus analysis of age-related macular degeneration.

[PMID 19696172] The involvement of complement factor B and complement component C2 in an Indian cohort with age-related macular degeneration.

[PMID 19707526 ] European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups.

[PMID 23864767 ] Association of CFH and CFB gene polymorphisms with retinopathy in type 2 diabetic patients

[PMID 22714898] Association of C2 and CFB polymorphisms with anterior uveitis.

[PMID 31916060] Investigation of genetic base in the treatment of age-related macular degeneration.