rs587776710
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587776710(-;GGG) |
Make rs587776710(GGG;GGG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 11890994 |
Gene | ETV6 |
is a | snp |
is | mentioned by |
dbSNP | rs587776710 |
dbSNP (classic) | rs587776710 |
ClinGen | rs587776710 |
ebi | rs587776710 |
HLI | rs587776710 |
Exac | rs587776710 |
Gnomad | rs587776710 |
Varsome | rs587776710 |
LitVar | rs587776710 |
Map | rs587776710 |
PheGenI | rs587776710 |
Biobank | rs587776710 |
1000 genomes | rs587776710 |
hgdp | rs587776710 |
ensembl | rs587776710 |
geneview | rs587776710 |
scholar | rs587776710 |
rs587776710 | |
pharmgkb | rs587776710 |
gwascentral | rs587776710 |
openSNP | rs587776710 |
23andMe | rs587776710 |
SNPshot | rs587776710 |
SNPdbe | rs587776710 |
MSV3d | rs587776710 |
GWAS Ctlg | rs587776710 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776710(GGG;GGG) |
Alt | rs587776710(GGG;GGG) |
Reference | Rs587776710(-;-) |
Significance | Pathogenic |
Disease | Acute myeloid leukemia |
Variation | info |
Gene | ETV6 |
CLNDBN | Acute myeloid leukemia |
Reversed | 0 |
HGVS | NC_000012.11:g.12043928_12043929insGGG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000009548.4, |