rs3753395
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3753395(A;A) |
Make rs3753395(A;T) |
Make rs3753395(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 196717522 |
Gene | CFH |
is a | snp |
is | mentioned by |
dbSNP | rs3753395 |
dbSNP (classic) | rs3753395 |
ClinGen | rs3753395 |
ebi | rs3753395 |
HLI | rs3753395 |
Exac | rs3753395 |
Gnomad | rs3753395 |
Varsome | rs3753395 |
LitVar | rs3753395 |
Map | rs3753395 |
PheGenI | rs3753395 |
Biobank | rs3753395 |
1000 genomes | rs3753395 |
hgdp | rs3753395 |
ensembl | rs3753395 |
geneview | rs3753395 |
scholar | rs3753395 |
rs3753395 | |
pharmgkb | rs3753395 |
gwascentral | rs3753395 |
openSNP | rs3753395 |
23andMe | rs3753395 |
SNPshot | rs3753395 |
SNPdbe | rs3753395 |
MSV3d | rs3753395 |
GWAS Ctlg | rs3753395 |
GMAF | 0.4582 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 23423485] Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China
[PMID 16936733] CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.
[PMID 25612476] Investigating the CFH Gene Polymorphisms as a Risk Factor for Age-related Macular Degeneration in an Iranian Population