rs779037308
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs779037308(A;A) |
Make rs779037308(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 10351093 |
Gene | TYK2 |
is a | snp |
is | mentioned by |
dbSNP | rs779037308 |
dbSNP (classic) | rs779037308 |
ClinGen | rs779037308 |
ebi | rs779037308 |
HLI | rs779037308 |
Exac | rs779037308 |
Gnomad | rs779037308 |
Varsome | rs779037308 |
LitVar | rs779037308 |
Map | rs779037308 |
PheGenI | rs779037308 |
Biobank | rs779037308 |
1000 genomes | rs779037308 |
hgdp | rs779037308 |
ensembl | rs779037308 |
geneview | rs779037308 |
scholar | rs779037308 |
rs779037308 | |
pharmgkb | rs779037308 |
gwascentral | rs779037308 |
openSNP | rs779037308 |
23andMe | rs779037308 |
SNPshot | rs779037308 |
SNPdbe | rs779037308 |
MSV3d | rs779037308 |
GWAS Ctlg | rs779037308 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs779037308(A;A) rs779037308(C;C) |
Alt | rs779037308(A;A) rs779037308(C;C) |
Reference | Rs779037308(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TYK2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.10461769G>A |
CLNSRC | |
CLNACC | RCV000489725.1, |