Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs142110773
rs142110773
DDC ; FIGNL1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs147030232
rs147030232
BBS2
A 0.700 CausalMutation CLINVAR

dbSNP: rs147484110
rs147484110
CSTB
G 0.700 CausalMutation CLINVAR

dbSNP: rs149830411
rs149830411
KANSL1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553196096
rs1553196096
CDC42
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553196101
rs1553196101
CDC42
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553196134
rs1553196134
CDC42
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553200431
rs1553200431
COL11A1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553511224
rs1553511224
TBR1
TC 0.700 GeneticVariation CLINVAR

dbSNP: rs1553538917
rs1553538917
SATB2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553763618
rs1553763618
POLR3GL
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554032789
rs1554032789
NIPBL
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554196416
rs1554196416
PHIP ; IRAK1BP1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554555063
rs1554555063
TMEM67
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554844486
rs1554844486
KAT6B
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554846212
rs1554846212
KAT6B ; DUPD1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554985320
rs1554985320
PAX6
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555038111
rs1555038111
KMT2A
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555103652
rs1555103652
GRIN2B
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555380716
rs1555380716
SLC12A6
GC 0.700 GeneticVariation CLINVAR

dbSNP: rs1555564126
rs1555564126
EFTUD2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555954284
rs1555954284
DDX3X
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1556165162
rs1556165162
HDAC8
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557045296
rs1557045296
SLC6A8
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1560092224
rs1560092224
ZBTB20
A 0.700 GeneticVariation CLINVAR