rs77375493, INSL6;JAK2

N. diseases: 187
Disease: Acute monocytic leukemia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
0.020 GeneticVariation BEFREE The JAK2 V617F mutation is frequently found in ET, while it is rare in de novo AML. 29979407 2018
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
0.020 GeneticVariation BEFREE We applied single nucleotide polymorphism arrays (SNP-A) to study karyotypic abnormalities in patients with atypical myeloproliferative syndromes (MPD), including myeloproliferative/myelodysplastic syndrome overlap both positive and negative for the JAK2 V617F mutation and secondary acute myeloid leukemia (AML). 18030353 2007