rs786205516
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs786205516(A;A) |
Make rs786205516(A;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 19 |
Position | 14410271 |
Gene | DDX39A |
is a | snp |
is | mentioned by |
dbSNP | rs786205516 |
dbSNP (classic) | rs786205516 |
ClinGen | rs786205516 |
ebi | rs786205516 |
HLI | rs786205516 |
Exac | rs786205516 |
Gnomad | rs786205516 |
Varsome | rs786205516 |
LitVar | rs786205516 |
Map | rs786205516 |
PheGenI | rs786205516 |
Biobank | rs786205516 |
1000 genomes | rs786205516 |
hgdp | rs786205516 |
ensembl | rs786205516 |
geneview | rs786205516 |
scholar | rs786205516 |
rs786205516 | |
pharmgkb | rs786205516 |
gwascentral | rs786205516 |
openSNP | rs786205516 |
23andMe | rs786205516 |
SNPshot | rs786205516 |
SNPdbe | rs786205516 |
MSV3d | rs786205516 |
GWAS Ctlg | rs786205516 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205516(A;A) |
Alt | rs786205516(A;A) |
Reference | Rs786205516(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | DDX39A |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000019.9:g.14521083A>T |
CLNSRC | |
CLNACC | RCV000171279.1, |