Gene: MED13L ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1135401765
rs1135401765
MED13L
A 0.700 CausalMutation CLINVAR

dbSNP: rs1135401766
rs1135401766
MED13L
TA 0.700 CausalMutation CLINVAR

dbSNP: rs1555243059
rs1555243059
MED13L
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555243582
rs1555243582
MED13L
T 0.700 CausalMutation CLINVAR