Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518770
rs1057518770
UBE3A ; SNHG14
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518813
rs1057518813
ERCC5 ; BIVM-ERCC5
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499549
rs1060499549
ZNF462
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555582065
rs1555582065
UBTF ; LOC101926967
T 0.700 CausalMutation CLINVAR

dbSNP: rs1569190079
rs1569190079
PDHA1
T 0.700 CausalMutation CLINVAR

dbSNP: rs267606826
rs267606826
FOXG1
A 0.700 CausalMutation CLINVAR

dbSNP: rs373145711
rs373145711
ASXL1
T 0.700 CausalMutation CLINVAR

dbSNP: rs587776954
rs587776954
C12orf57 ; RNU7-1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs77078070
rs77078070
KLHL7
T 0.700 GeneticVariation CLINVAR

dbSNP: rs875989800
rs875989800
SMARCB1
G 0.700 CausalMutation CLINVAR