rs1059046
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1059046(A;A) |
Make rs1059046(A;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 79559458 |
Gene | SFTPA2 |
is a | snp |
is | mentioned by |
dbSNP | rs1059046 |
dbSNP (classic) | rs1059046 |
ClinGen | rs1059046 |
ebi | rs1059046 |
HLI | rs1059046 |
Exac | rs1059046 |
Gnomad | rs1059046 |
Varsome | rs1059046 |
LitVar | rs1059046 |
Map | rs1059046 |
PheGenI | rs1059046 |
Biobank | rs1059046 |
1000 genomes | rs1059046 |
hgdp | rs1059046 |
ensembl | rs1059046 |
geneview | rs1059046 |
scholar | rs1059046 |
rs1059046 | |
pharmgkb | rs1059046 |
gwascentral | rs1059046 |
openSNP | rs1059046 |
23andMe | rs1059046 |
SNPshot | rs1059046 |
SNPdbe | rs1059046 |
MSV3d | rs1059046 |
GWAS Ctlg | rs1059046 |
Max Magnitude | 0 |
[PMID 24950659] Surfactant protein A genetic variants associate with severe respiratory insufficiency in pandemic influenza A virus infection
ClinVar | |
---|---|
Risk | rs1059046(A;A) rs1059046(G;G) |
Alt | rs1059046(A;A) rs1059046(G;G) |
Reference | Rs1059046(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | SFTPA2 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000010.10:g.81319214G>T |
CLNSRC | |
CLNACC | RCV000221077.1, |