rs4151657

Orientation

plus

Stabilized

plus

Make rs4151657(C;C)

Make rs4151657(C;T)

Make rs4151657(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31949763

Gene

CFB

is a	snp
is	mentioned by
dbSNP	rs4151657
dbSNP (classic)	rs4151657
ClinGen	rs4151657
ebi	rs4151657
HLI	rs4151657
Exac	rs4151657
Gnomad	rs4151657
Varsome	rs4151657
LitVar	rs4151657
Map	rs4151657
PheGenI	rs4151657
Biobank	rs4151657
1000 genomes	rs4151657
hgdp	rs4151657
ensembl	rs4151657
geneview	rs4151657
scholar	rs4151657
google	rs4151657
pharmgkb	rs4151657
gwascentral	rs4151657
openSNP	rs4151657
23andMe	rs4151657
SNPshot	rs4151657
SNPdbe	rs4151657
MSV3d	rs4151657
GWAS Ctlg	rs4151657

GMAF

0.2865

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[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.

GWAS snp
PMID	[PMID 24837172]
Trait	Ulcerative colitis
Title	Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis.
Risk Allele	G
P-val	5E-14
Odds Ratio	1.54 [1.38-1.73]

[PMID 27759029] A cross-ethnic survey of CFB and SLC44A4, Indian ulcerative colitis GWAS hits, underscores their potential role in disease susceptibility.

[PMID 29551506] Genome-wide association study in ethnic Russians suggests an association of the MHC class III genomic region with the risk of primary varicose veins.