rs786205154
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AACAG;AACAG) | 0 | common in clinvar |
Make rs786205154(-;-) |
Make rs786205154(-;AACAG) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 11885921 |
Gene | ETV6 |
is a | snp |
is | mentioned by |
dbSNP | rs786205154 |
dbSNP (classic) | rs786205154 |
ClinGen | rs786205154 |
ebi | rs786205154 |
HLI | rs786205154 |
Exac | rs786205154 |
Gnomad | rs786205154 |
Varsome | rs786205154 |
LitVar | rs786205154 |
Map | rs786205154 |
PheGenI | rs786205154 |
Biobank | rs786205154 |
1000 genomes | rs786205154 |
hgdp | rs786205154 |
ensembl | rs786205154 |
geneview | rs786205154 |
scholar | rs786205154 |
rs786205154 | |
pharmgkb | rs786205154 |
gwascentral | rs786205154 |
openSNP | rs786205154 |
23andMe | rs786205154 |
SNPshot | rs786205154 |
SNPdbe | rs786205154 |
MSV3d | rs786205154 |
GWAS Ctlg | rs786205154 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786205154(-;-) |
Alt | rs786205154(-;-) |
Reference | Rs786205154(AACAG;AACAG) |
Significance | Pathogenic |
Disease | See cases Acute lymphoid leukemia Thrombocytopenia Inborn genetic diseases |
Variation | info |
Gene | ETV6 |
CLNDBN | See cases Acute lymphoid leukemia Thrombocytopenia Inborn genetic diseases |
Reversed | 0 |
HGVS | NC_000012.11:g.12038855_12038859delAACAG |
CLNSRC | |
CLNACC | RCV000170463.1, RCV000170466.1, RCV000170467.1, RCV000210685.1, |