Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1034395178
rs1034395178
A 0.700 CausalMutation CLINVAR Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants. 29469822

2018

dbSNP: rs1469540056
rs1469540056
C 0.700 GeneticVariation CLINVAR

dbSNP: rs189150283
rs189150283
T 0.700 CausalMutation CLINVAR