rs773590163
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs773590163(A;A) |
Make rs773590163(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 17843169 |
Gene | JAK3 |
is a | snp |
is | mentioned by |
dbSNP | rs773590163 |
dbSNP (classic) | rs773590163 |
ClinGen | rs773590163 |
ebi | rs773590163 |
HLI | rs773590163 |
Exac | rs773590163 |
Gnomad | rs773590163 |
Varsome | rs773590163 |
LitVar | rs773590163 |
Map | rs773590163 |
PheGenI | rs773590163 |
Biobank | rs773590163 |
1000 genomes | rs773590163 |
hgdp | rs773590163 |
ensembl | rs773590163 |
geneview | rs773590163 |
scholar | rs773590163 |
rs773590163 | |
pharmgkb | rs773590163 |
gwascentral | rs773590163 |
openSNP | rs773590163 |
23andMe | rs773590163 |
SNPshot | rs773590163 |
SNPdbe | rs773590163 |
MSV3d | rs773590163 |
GWAS Ctlg | rs773590163 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs773590163(A;A) |
Alt | rs773590163(A;A) |
Reference | Rs773590163(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | JAK3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.17953978G>A |
CLNSRC | |
CLNACC | RCV000479086.1, |