rs373359894
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs373359894(A;A) |
Make rs373359894(A;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 120997684 |
Gene | C5 |
is a | snp |
is | mentioned by |
dbSNP | rs373359894 |
dbSNP (classic) | rs373359894 |
ClinGen | rs373359894 |
ebi | rs373359894 |
HLI | rs373359894 |
Exac | rs373359894 |
Gnomad | rs373359894 |
Varsome | rs373359894 |
LitVar | rs373359894 |
Map | rs373359894 |
PheGenI | rs373359894 |
Biobank | rs373359894 |
1000 genomes | rs373359894 |
hgdp | rs373359894 |
ensembl | rs373359894 |
geneview | rs373359894 |
scholar | rs373359894 |
rs373359894 | |
pharmgkb | rs373359894 |
gwascentral | rs373359894 |
openSNP | rs373359894 |
23andMe | rs373359894 |
SNPshot | rs373359894 |
SNPdbe | rs373359894 |
MSV3d | rs373359894 |
GWAS Ctlg | rs373359894 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs373359894(A;A) rs373359894(T;T) |
Alt | rs373359894(A;A) rs373359894(T;T) |
Reference | Rs373359894(G;G) |
Significance | Other |
Disease | Eculizumab |
Variation | info |
Gene | C5 |
CLNDBN | Eculizumab, poor response to |
Reversed | 0 |
HGVS | NC_000009.11:g.123759962G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000114935.4, |