Gene: ASXL3 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555743003
rs1555743003
ASXL3
A 0.700 CausalMutation CLINVAR Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome. 27075689

2016
dbSNP: rs1057519498
rs1057519498
ASXL3
TC 0.700 CausalMutation CLINVAR

dbSNP: rs1060499602
rs1060499602
ASXL3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1064793765
rs1064793765
ASXL3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1131691668
rs1131691668
ASXL3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1179499890
rs1179499890
ASXL3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555742148
rs1555742148
ASXL3
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1555742167
rs1555742167
ASXL3
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1555742500
rs1555742500
ASXL3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555744039
rs1555744039
ASXL3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555744086
rs1555744086
ASXL3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555744282
rs1555744282
ASXL3
T 0.700 CausalMutation CLINVAR

dbSNP: rs1568359734
rs1568359734
ASXL3
G 0.700 CausalMutation CLINVAR

dbSNP: rs587777061
rs587777061
ASXL3
T 0.700 CausalMutation CLINVAR

dbSNP: rs587777062
rs587777062
ASXL3
T 0.700 CausalMutation CLINVAR

dbSNP: rs797045317
rs797045317
ASXL3
C 0.700 CausalMutation CLINVAR

dbSNP: rs869312696
rs869312696
ASXL3
A 0.700 CausalMutation CLINVAR