Gene: KIF1A ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs672601368
rs672601368
KIF1A
T 0.700 CausalMutation CLINVAR De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome. 26486474

2016
dbSNP: rs387906799
rs387906799
KIF1A
A 0.700 CausalMutation CLINVAR

dbSNP: rs672601362
rs672601362
KIF1A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs672601363
rs672601363
KIF1A
T 0.700 GeneticVariation CLINVAR

dbSNP: rs672601367
rs672601367
KIF1A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs672601369
rs672601369
KIF1A
T 0.700 CausalMutation CLINVAR

dbSNP: rs672601370
rs672601370
KIF1A
A 0.700 GeneticVariation CLINVAR