Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1010184002
rs1010184002
PEX6
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518972
rs1057518972
TRPS1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1223073957
rs1223073957
MED25
A 0.700 CausalMutation CLINVAR

dbSNP: rs137854889
rs137854889
ZMPSTE24
GT 0.700 CausalMutation CLINVAR

dbSNP: rs1555548678
rs1555548678
STAT5B
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555548680
rs1555548680
STAT5B
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555549674
rs1555549674
STAT5B
G 0.700 CausalMutation CLINVAR

dbSNP: rs267606826
rs267606826
FOXG1
A 0.700 CausalMutation CLINVAR

dbSNP: rs375817528
rs375817528
CAPN1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs61753219
rs61753219
PEX6
A 0.700 GeneticVariation CLINVAR

dbSNP: rs776291104
rs776291104
MED25
T 0.700 GeneticVariation CLINVAR