rs121913449
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs121913449(A;T) |
Make rs121913449(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 130862977 |
Gene | ABL1 |
is a | snp |
is | mentioned by |
dbSNP | rs121913449 |
dbSNP (classic) | rs121913449 |
ClinGen | rs121913449 |
ebi | rs121913449 |
HLI | rs121913449 |
Exac | rs121913449 |
Gnomad | rs121913449 |
Varsome | rs121913449 |
LitVar | rs121913449 |
Map | rs121913449 |
PheGenI | rs121913449 |
Biobank | rs121913449 |
1000 genomes | rs121913449 |
hgdp | rs121913449 |
ensembl | rs121913449 |
geneview | rs121913449 |
scholar | rs121913449 |
rs121913449 | |
pharmgkb | rs121913449 |
gwascentral | rs121913449 |
openSNP | rs121913449 |
23andMe | rs121913449 |
SNPshot | rs121913449 |
SNPdbe | rs121913449 |
MSV3d | rs121913449 |
GWAS Ctlg | rs121913449 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121913449(T;T) |
Alt | rs121913449(T;T) |
Reference | Rs121913449(A;A) |
Significance | Probable-Pathogenic |
Disease | Chronic myeloid leukemia |
Variation | info |
Gene | ABL1 |
CLNDBN | Chronic myeloid leukemia |
Reversed | 0 |
HGVS | NC_000009.11:g.133738364A>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000443466.1, |