Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555889984
rs1555889984
RUNX1
A 0.700 CausalMutation CLINVAR A novel germline RUNX1 mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from India. 30990344

2019
dbSNP: rs1555889984
rs1555889984
RUNX1
A 0.700 GeneticVariation CLINVAR