Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555038029
rs1555038029
KMT2A
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555452127
rs1555452127
ALG1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555640521
rs1555640521
LAMA1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1557781252
rs1557781252
GATAD2B
A 0.700 CausalMutation CLINVAR

dbSNP: rs1560755661
rs1560755661
TBCK
A 0.700 CausalMutation CLINVAR

dbSNP: rs1562114190
rs1562114190
PHIP ; IRAK1BP1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1562127631
rs1562127631
PHIP ; IRAK1BP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1562150844
rs1562150844
PHIP
C 0.700 CausalMutation CLINVAR

dbSNP: rs1562203136
rs1562203136
PHIP
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1563183492
rs1563183492
AUTS2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1567941252
rs1567941252
PCGF2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1569324457
rs1569324457
ASXL1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1569548274
rs1569548274
MECP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs199469465
rs199469465
SRCAP
T 0.700 CausalMutation CLINVAR

dbSNP: rs201439531
rs201439531
CHAT
G 0.700 CausalMutation CLINVAR

dbSNP: rs201943194
rs201943194
DNAH11
T 0.700 CausalMutation CLINVAR

dbSNP: rs267606826
rs267606826
FOXG1
A 0.700 CausalMutation CLINVAR

dbSNP: rs369160589
rs369160589
ALG1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs387906702
rs387906702
SMC1A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs397515415
rs397515415
HDAC8
A 0.700 CausalMutation CLINVAR

dbSNP: rs398122394
rs398122394
ALG13
G 0.700 CausalMutation CLINVAR

dbSNP: rs559979281
rs559979281
CLASP1 ; RNU4ATAC ; LOC107985942
T 0.700 CausalMutation CLINVAR

dbSNP: rs587777893
rs587777893
MTOR
A 0.700 CausalMutation CLINVAR

dbSNP: rs751093906
rs751093906
SLC20A2
A 0.700 CausalMutation CLINVAR

dbSNP: rs769234940
rs769234940
CHAT
T 0.700 CausalMutation CLINVAR