Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554603293
rs1554603293
CHD7
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555043939
rs1555043939
KMT2A
AG 0.700 CausalMutation CLINVAR

dbSNP: rs1555565774
rs1555565774
EFTUD2
T 0.700 CausalMutation CLINVAR