Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205133
rs786205133
RLIM
C 0.700 GeneticVariation CLINVAR Syndromic X-linked intellectual disability segregating with a missense variant in RLIM. 25735484

2015
dbSNP: rs1569118680
rs1569118680
NLGN4X
G 0.700 CausalMutation CLINVAR