rs7540032
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7540032(C;C) |
Make rs7540032(C;T) |
Make rs7540032(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 196732154 |
Gene | CFH |
is a | snp |
is | mentioned by |
dbSNP | rs7540032 |
dbSNP (classic) | rs7540032 |
ClinGen | rs7540032 |
ebi | rs7540032 |
HLI | rs7540032 |
Exac | rs7540032 |
Gnomad | rs7540032 |
Varsome | rs7540032 |
LitVar | rs7540032 |
Map | rs7540032 |
PheGenI | rs7540032 |
Biobank | rs7540032 |
1000 genomes | rs7540032 |
hgdp | rs7540032 |
ensembl | rs7540032 |
geneview | rs7540032 |
scholar | rs7540032 |
rs7540032 | |
pharmgkb | rs7540032 |
gwascentral | rs7540032 |
openSNP | rs7540032 |
23andMe | rs7540032 |
SNPshot | rs7540032 |
SNPdbe | rs7540032 |
MSV3d | rs7540032 |
GWAS Ctlg | rs7540032 |
GMAF | 0.4408 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 21882633] [Influence of genetic mutations on clinical presentation of subretinal neovascularization. Report 1: The impact of CFH and IL-8 genes polymorphism]