rs541862
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common on affy axiom data |
Make rs541862(A;G) |
Make rs541862(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31949174 |
Gene | CFB |
is a | snp |
is | mentioned by |
dbSNP | rs541862 |
dbSNP (classic) | rs541862 |
ClinGen | rs541862 |
ebi | rs541862 |
HLI | rs541862 |
Exac | rs541862 |
Gnomad | rs541862 |
Varsome | rs541862 |
LitVar | rs541862 |
Map | rs541862 |
PheGenI | rs541862 |
Biobank | rs541862 |
1000 genomes | rs541862 |
hgdp | rs541862 |
ensembl | rs541862 |
geneview | rs541862 |
scholar | rs541862 |
rs541862 | |
pharmgkb | rs541862 |
gwascentral | rs541862 |
openSNP | rs541862 |
23andMe | rs541862 |
SNPshot | rs541862 |
SNPdbe | rs541862 |
MSV3d | rs541862 |
GWAS Ctlg | rs541862 |
GMAF | 0.09963 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22694956![]() |
Trait | |
Title | Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3. |
Risk Allele | T |
P-val | 9E-17 |
Odds Ratio | 1.8900 None |
[PMID 22232432] Significance of C2/CFB variants in age-related macular degeneration and polypoidal choroidal vasculopathy in a Japanese population.