Gene: BSCL2 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852972
rs137852972
BSCL2 ; HNRNPUL2-BSCL2
C 0.840 CausalMutation CLINVAR

dbSNP: rs137852973
rs137852973
BSCL2 ; HNRNPUL2-BSCL2
A 0.820 CausalMutation CLINVAR