rs143334143
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 1.9 | Higher (1.9x) risk for COVID-19 illness being severe |
(G;G) | 0 | common/normal |
Make rs143334143(A;A) |
is a | snp |
is | mentioned by |
dbSNP | rs143334143 |
dbSNP (classic) | rs143334143 |
ClinGen | rs143334143 |
ebi | rs143334143 |
HLI | rs143334143 |
Exac | rs143334143 |
Gnomad | rs143334143 |
Varsome | rs143334143 |
LitVar | rs143334143 |
Map | rs143334143 |
PheGenI | rs143334143 |
Biobank | rs143334143 |
1000 genomes | rs143334143 |
hgdp | rs143334143 |
ensembl | rs143334143 |
geneview | rs143334143 |
scholar | rs143334143 |
rs143334143 | |
pharmgkb | rs143334143 |
gwascentral | rs143334143 |
openSNP | rs143334143 |
23andMe | rs143334143 |
SNPshot | rs143334143 |
SNPdbe | rs143334143 |
MSV3d | rs143334143 |
GWAS Ctlg | rs143334143 |
Max Magnitude | 1.9 |
Genetic mechanisms of critical illness in Covid-19 [1]; moderate increase (1.9x) for risk of becoming critically ill upon COVID-19 infection for carriers of the minor (A) allele
Note this SNP is tightly linked to, and presumably reflecting the same risk factor as two SNPs that are commonly found on DNA chips used by companies such as MyHeritage or Ancestry, rs130072 and also rs2073724; in the FWD (plus) orientation, the minor alleles for those SNPs are both T (and the major, non-risk allele is C).