Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057521223
rs1057521223
SCN2A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057524820
rs1057524820
SCN8A
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060499733
rs1060499733
DHX30
G 0.700 CausalMutation CLINVAR

dbSNP: rs1064793575
rs1064793575
SLC9A6
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307845
rs1085307845
PHIP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1131692231
rs1131692231
CYFIP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1380822792
rs1380822792
NAA15
A 0.700 CausalMutation CLINVAR

dbSNP: rs142110773
rs142110773
DDC ; FIGNL1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1448259271
rs1448259271
IRF2BPL ; LOC107984638
A 0.700 GeneticVariation CLINVAR

dbSNP: rs146539065
rs146539065
SEPSECS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs148881970
rs148881970
NAGLU
G 0.700 CausalMutation CLINVAR

dbSNP: rs1554317002
rs1554317002
CDK13 ; LOC112267983
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554888939
rs1554888939
EHMT1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555358382
rs1555358382
GCH1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555462347
rs1555462347
USP7
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555939456
rs1555939456
RPS6KA3
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1562114190
rs1562114190
PHIP ; IRAK1BP1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1562171209
rs1562171209
PHIP
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1564421528
rs1564421528
WAC
T 0.700 CausalMutation CLINVAR

dbSNP: rs1567010427
rs1567010427
DYNC1H1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs200661329
rs200661329
PIGQ
A 0.700 GeneticVariation CLINVAR

dbSNP: rs267606826
rs267606826
FOXG1
A 0.700 CausalMutation CLINVAR

dbSNP: rs281864996
rs281864996
GNPTAB
ATTTTC 0.700 GeneticVariation CLINVAR

dbSNP: rs370717845
rs370717845
HGSNAT
A 0.700 CausalMutation CLINVAR

dbSNP: rs397507562
rs397507562
GNPTAB
T 0.700 GeneticVariation CLINVAR