Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777644
rs587777644
METTL23
C 0.700 CausalMutation CLINVAR Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability. 24626631

2014
dbSNP: rs587777644
rs587777644
METTL23
C 0.700 CausalMutation CLINVAR METTL23, a transcriptional partner of GABPA, is essential for human cognition. 24501276

2014