Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs606231473
rs606231473
A 0.800 CausalMutation CLINVAR

dbSNP: rs138156467
rs138156467
T 0.700 CausalMutation CLINVAR GM-CSF stimulates granulopoiesis in a congenital neutropenia patient with loss-of-function biallelic heterozygous CSF3R mutations. 26324699

2015

dbSNP: rs606231474
rs606231474
T 0.700 CausalMutation CLINVAR

dbSNP: rs606231475
rs606231475
T 0.700 CausalMutation CLINVAR

dbSNP: rs759302795
rs759302795
T 0.700 CausalMutation CLINVAR

dbSNP: rs879253750
rs879253750
A 0.700 CausalMutation CLINVAR

dbSNP: rs890101650
rs890101650
AC 0.700 CausalMutation CLINVAR