rs35018800
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs35018800(A;A) |
Make rs35018800(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 10354167 |
Gene | TYK2 |
is a | snp |
is | mentioned by |
dbSNP | rs35018800 |
dbSNP (classic) | rs35018800 |
ClinGen | rs35018800 |
ebi | rs35018800 |
HLI | rs35018800 |
Exac | rs35018800 |
Gnomad | rs35018800 |
Varsome | rs35018800 |
LitVar | rs35018800 |
Map | rs35018800 |
PheGenI | rs35018800 |
Biobank | rs35018800 |
1000 genomes | rs35018800 |
hgdp | rs35018800 |
ensembl | rs35018800 |
geneview | rs35018800 |
scholar | rs35018800 |
rs35018800 | |
pharmgkb | rs35018800 |
gwascentral | rs35018800 |
openSNP | rs35018800 |
23andMe | rs35018800 |
SNPshot | rs35018800 |
SNPdbe | rs35018800 |
MSV3d | rs35018800 |
GWAS Ctlg | rs35018800 |
Max Magnitude | 0 |
[PMID 26338038] Influence of TYK2 in systemic sclerosis susceptibility: a new locus in the IL-12 pathway
ClinVar | |
---|---|
Risk | rs35018800(A;A) |
Alt | rs35018800(A;A) |
Reference | Rs35018800(G;G) |
Significance | Probable-non-pathogenic |
Disease | not specified |
Variation | info |
Gene | TYK2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000019.9:g.10464843G>A |
CLNSRC | |
CLNACC | RCV000284384.1, |