Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907113
rs387907113
NBEAL2
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome 		C 0.800 CausalMutation CLINVAR

dbSNP: rs387907114
rs387907114
NBEAL2
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome 		T 0.800 CausalMutation CLINVAR

dbSNP: rs387907115
rs387907115
NBEAL2
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome 		T 0.800 CausalMutation CLINVAR

dbSNP: rs1553659758
rs1553659758
NBEAL2
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1553663498
rs1553663498
NBEAL2
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs372277612
rs372277612
NBEAL2
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs387907112
rs387907112
NBEAL2
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs794726682
rs794726682
NBEAL2
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs794726683
rs794726683
NBEAL2
CUI: C0272302
Disease: Gray Platelet Syndrome
Gray Platelet Syndrome 		TG 0.700 CausalMutation CLINVAR