Gene: SLFN14 ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757188030
rs757188030
SLFN14
0.800 GeneticVariation UNIPROT SLFN14-related thrombocytopenia: identification within a large series of patients with inherited thrombocytopenia. 26769223

2016
dbSNP: rs869320714
rs869320714
SLFN14
0.800 GeneticVariation UNIPROT SLFN14-related thrombocytopenia: identification within a large series of patients with inherited thrombocytopenia. 26769223

2016
dbSNP: rs869320715
rs869320715
SLFN14
0.800 GeneticVariation UNIPROT SLFN14-related thrombocytopenia: identification within a large series of patients with inherited thrombocytopenia. 26769223

2016
dbSNP: rs869320716
rs869320716
SLFN14
0.800 GeneticVariation UNIPROT SLFN14-related thrombocytopenia: identification within a large series of patients with inherited thrombocytopenia. 26769223

2016
dbSNP: rs757188030
rs757188030
SLFN14
0.800 GeneticVariation UNIPROT SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects. 26280575

2015
dbSNP: rs869320714
rs869320714
SLFN14
0.800 GeneticVariation UNIPROT SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects. 26280575

2015
dbSNP: rs869320715
rs869320715
SLFN14
0.800 GeneticVariation UNIPROT SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects. 26280575

2015
dbSNP: rs869320716
rs869320716
SLFN14
0.800 GeneticVariation UNIPROT SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects. 26280575

2015
dbSNP: rs757188030
rs757188030
SLFN14
A 0.800 CausalMutation CLINVAR

dbSNP: rs869320714
rs869320714
SLFN14
T 0.800 CausalMutation CLINVAR

dbSNP: rs869320715
rs869320715
SLFN14
A 0.800 CausalMutation CLINVAR

dbSNP: rs869320716
rs869320716
SLFN14
C 0.800 CausalMutation CLINVAR