Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131692231
rs1131692231
CYFIP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs113871094
rs113871094
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1202430946
rs1202430946
IGHMBP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs121918459
rs121918459
PTPN11
G 0.700 CausalMutation CLINVAR

dbSNP: rs132630297
rs132630297
PHF6
T 0.700 CausalMutation CLINVAR

dbSNP: rs1448259271
rs1448259271
IRF2BPL ; LOC107984638
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1554317002
rs1554317002
CDK13 ; LOC112267983
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555178899
rs1555178899
WNT1 ; WNT10B
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555247672
rs1555247672
MED13L
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555939456
rs1555939456
RPS6KA3
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557179325
rs1557179325
FLNA
T 0.700 CausalMutation CLINVAR

dbSNP: rs1567263168
rs1567263168
CREBBP
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1568070621
rs1568070621
BPTF
G 0.700 CausalMutation CLINVAR

dbSNP: rs751569508
rs751569508
NCOR1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs886040971
rs886040971
TRPS1
A 0.700 CausalMutation CLINVAR