Gene: BSCL2 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777606
rs587777606
BSCL2 ; LRRN4CL ; HNRNPUL2-BSCL2
A 0.720 CausalMutation CLINVAR

dbSNP: rs587777607
rs587777607
BSCL2 ; HNRNPUL2-BSCL2
A 0.700 CausalMutation CLINVAR

dbSNP: rs587777608
rs587777608
BSCL2 ; HNRNPUL2-BSCL2
C 0.700 CausalMutation CLINVAR