Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518868
rs1057518868
FOXF1 ; FENDRR
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518914
rs1057518914
RPS6KA3
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1114167294
rs1114167294
FOXP4
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1163944538
rs1163944538
TMEM94
GA 0.700 CausalMutation CLINVAR

dbSNP: rs121918455
rs121918455
PTPN11
G 0.700 CausalMutation CLINVAR

dbSNP: rs1294950721
rs1294950721
JAG1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1352010373
rs1352010373
TMEM94
C 0.700 CausalMutation CLINVAR

dbSNP: rs142239530
rs142239530
STIM1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs143044921
rs143044921
FREM2
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs1554643168
rs1554643168
PUF60
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1554643168
rs1554643168
PUF60
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555038029
rs1555038029
KMT2A
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555226315
rs1555226315
TBX5
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555564126
rs1555564126
EFTUD2
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555565774
rs1555565774
EFTUD2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557612048
rs1557612048
ARID1A
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1564062144
rs1564062144
HNRNPK
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1565569158
rs1565569158
ATN1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs180177039
rs180177039
BRAF
C 0.700 GeneticVariation CLINVAR

dbSNP: rs431905509
rs431905509
SLC25A1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs483352822
rs483352822
RIT1
G 0.700 CausalMutation CLINVAR

dbSNP: rs61729366
rs61729366
FRAS1
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs746800707
rs746800707
AAR2
A 0.700 GeneticVariation CLINVAR

dbSNP: rs755246809
rs755246809
AHI1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs759125480
rs759125480
CEP120
A 0.700 GeneticVariation CLINVAR