rs10922153
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs10922153(G;G) |
Make rs10922153(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 197009485 |
Gene | CFHR5 |
is a | snp |
is | mentioned by |
dbSNP | rs10922153 |
dbSNP (classic) | rs10922153 |
ClinGen | rs10922153 |
ebi | rs10922153 |
HLI | rs10922153 |
Exac | rs10922153 |
Gnomad | rs10922153 |
Varsome | rs10922153 |
LitVar | rs10922153 |
Map | rs10922153 |
PheGenI | rs10922153 |
Biobank | rs10922153 |
1000 genomes | rs10922153 |
hgdp | rs10922153 |
ensembl | rs10922153 |
geneview | rs10922153 |
scholar | rs10922153 |
rs10922153 | |
pharmgkb | rs10922153 |
gwascentral | rs10922153 |
openSNP | rs10922153 |
23andMe | rs10922153 |
SNPshot | rs10922153 |
SNPdbe | rs10922153 |
MSV3d | rs10922153 |
GWAS Ctlg | rs10922153 |
GMAF | 0.3173 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 23582991] Genetic Influences on the Outcome of Anti-Vascular Endothelial Growth Factor Treatment in Neovascular Age-related Macular Degeneration
[PMID 18541031] The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.
[PMID 19801603] Rapid inexpensive genome-wide association using pooled whole blood.
ClinVar | |
---|---|
Risk | rs10922153(G;G) |
Alt | rs10922153(G;G) |
Reference | Rs10922153(T;T) |
Significance | Non-pathogenic |
Disease | Mesangiocapillary glomerulonephritis |
Variation | info |
Gene | CFHR5 |
CLNDBN | Mesangiocapillary glomerulonephritis, type II |
Reversed | 0 |
HGVS | NC_000001.10:g.196978615T>G |
CLNSRC | |
CLNACC | RCV000294081.1, |