rs864321619
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs864321619(-;CGTTGATTTCAGAGAATATGA) |
Make rs864321619(CGTTGATTTCAGAGAATATGA;CGTTGATTTCAGAGAATATGA) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 13 |
Position | 28034125 |
Gene | FLT3 |
is a | snp |
is | mentioned by |
dbSNP | rs864321619 |
dbSNP (classic) | rs864321619 |
ClinGen | rs864321619 |
ebi | rs864321619 |
HLI | rs864321619 |
Exac | rs864321619 |
Gnomad | rs864321619 |
Varsome | rs864321619 |
LitVar | rs864321619 |
Map | rs864321619 |
PheGenI | rs864321619 |
Biobank | rs864321619 |
1000 genomes | rs864321619 |
hgdp | rs864321619 |
ensembl | rs864321619 |
geneview | rs864321619 |
scholar | rs864321619 |
rs864321619 | |
pharmgkb | rs864321619 |
gwascentral | rs864321619 |
openSNP | rs864321619 |
23andMe | rs864321619 |
SNPshot | rs864321619 |
SNPdbe | rs864321619 |
MSV3d | rs864321619 |
GWAS Ctlg | rs864321619 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs864321619(CGTTGATTTCAGAGAATATGA;CGTTGATTTCAGAGAATATGA) |
Alt | rs864321619(CGTTGATTTCAGAGAATATGA;CGTTGATTTCAGAGAATATGA) |
Reference | Rs864321619(-;-) |
Significance | Pathogenic |
Disease | Myelodysplastic syndrome progressed to acute myeloid leukemia |
Variation | info |
Gene | FLT3 |
CLNDBN | Myelodysplastic syndrome progressed to acute myeloid leukemia |
Reversed | 1 |
HGVS | NC_000013.10:g.28608263_28608283dup21 |
CLNSRC | |
CLNACC | RCV000203482.1, |