Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518914
rs1057518914
RPS6KA3
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519334
rs1057519334
NPR2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1057519946
rs1057519946
PPP2R1A
T 0.700 GeneticVariation CLINVAR

dbSNP: rs112795301
rs112795301
FOXP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121908425
rs121908425
CRMP1 ; EVC
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913355
rs121913355
BRAF
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918494
rs121918494
FGFR2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1276519904
rs1276519904
H3-3A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1364709483
rs1364709483
TBX2 ; TBX2-AS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553525325
rs1553525325
SCN1A ; SCN1A-AS1 ; LOC102724058
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554110735
rs1554110735
TFAP2A
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554196416
rs1554196416
PHIP ; IRAK1BP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554199368
rs1554199368
NSD1
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554603293
rs1554603293
CHD7
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554691658
rs1554691658
PTCH1
GGGTCCACAACATCT 0.700 GeneticVariation CLINVAR

dbSNP: rs1554700718
rs1554700718
HNRNPK
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555038111
rs1555038111
KMT2A
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555350397
rs1555350397
OTX2
CC 0.700 GeneticVariation CLINVAR

dbSNP: rs1555380716
rs1555380716
SLC12A6
GC 0.700 GeneticVariation CLINVAR

dbSNP: rs1555528356
rs1555528356
ANKRD11
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555565774
rs1555565774
EFTUD2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555741826
rs1555741826
PRR12
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555954284
rs1555954284
DDX3X
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1556955128
rs1556955128
HUWE1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557045296
rs1557045296
SLC6A8
T 0.700 GeneticVariation CLINVAR