Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1562134961
rs1562134961
PHIP ; IRAK1BP1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1562171209
rs1562171209
PHIP
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1563183492
rs1563183492
AUTS2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1566823361
rs1566823361
FGF14
TG 0.700 GeneticVariation CLINVAR

dbSNP: rs1567574466
rs1567574466
ANKRD11
T 0.700 CausalMutation CLINVAR

dbSNP: rs1567941252
rs1567941252
PCGF2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1568019012
rs1568019012
LAMA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1568070621
rs1568070621
BPTF
G 0.700 CausalMutation CLINVAR

dbSNP: rs1568507354
rs1568507354
RYR1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1569149539
rs1569149539
TCF20
C 0.700 CausalMutation CLINVAR

dbSNP: rs1569151204
rs1569151204
TCF20
A 0.700 CausalMutation CLINVAR

dbSNP: rs1569525894
rs1569525894
SLC9A6
A 0.700 GeneticVariation CLINVAR

dbSNP: rs267608327
rs267608327
MECP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs28935468
rs28935468
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397514627
rs397514627
CAMK2G
G 0.700 GeneticVariation CLINVAR

dbSNP: rs398124401
rs398124401
SRD5A3
A 0.700 CausalMutation CLINVAR

dbSNP: rs555145190
rs555145190
NAGLU
T 0.700 CausalMutation CLINVAR

dbSNP: rs587784105
rs587784105
NSD1
A 0.700 CausalMutation CLINVAR

dbSNP: rs61750240
rs61750240
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs62643608
rs62643608
CDKL5
C 0.700 CausalMutation CLINVAR

dbSNP: rs757511770
rs757511770
FMN2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs765379963
rs765379963
TMCO1
A 0.700 CausalMutation CLINVAR

dbSNP: rs768407867
rs768407867
CHRNA1
T 0.700 CausalMutation CLINVAR

dbSNP: rs794726827
rs794726827
SCN1A ; SCN1A-AS1
T 0.700 CausalMutation CLINVAR

dbSNP: rs796052571
rs796052571
GRIN2B ; LOC105369668
T 0.700 GeneticVariation CLINVAR