Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131692272
rs1131692272
T 0.700 CausalMutation CLINVAR

dbSNP: rs886041125
rs886041125
G 0.700 CausalMutation CLINVAR

dbSNP: rs886040958
rs886040958
A 0.700 CausalMutation CLINVAR

dbSNP: rs730882201
rs730882201
A 0.700 GeneticVariation CLINVAR

dbSNP: rs869312696
rs869312696
A 0.700 CausalMutation CLINVAR

dbSNP: rs147030232
rs147030232
A 0.700 CausalMutation CLINVAR

dbSNP: rs797045412
rs797045412
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1135402760
rs1135402760
C 0.700 GeneticVariation CLINVAR Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder. 30879638

2019

dbSNP: rs730882202
rs730882202
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1553196096
rs1553196096
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553196101
rs1553196101
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553196134
rs1553196134
T 0.700 CausalMutation CLINVAR

dbSNP: rs1565977796
rs1565977796
A 0.700 CausalMutation CLINVAR

dbSNP: rs773722162
rs773722162
TGAGGAGGAAGAA 0.700 GeneticVariation CLINVAR

dbSNP: rs367557471
rs367557471
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1553200431
rs1553200431
G 0.700 GeneticVariation CLINVAR

dbSNP: rs147484110
rs147484110
G 0.700 CausalMutation CLINVAR

dbSNP: rs121434616
rs121434616
A 0.700 CausalMutation CLINVAR

dbSNP: rs142110773
rs142110773
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555954284
rs1555954284
T 0.700 GeneticVariation CLINVAR

dbSNP: rs752738546
rs752738546
T 0.700 CausalMutation CLINVAR

dbSNP: rs875989802
rs875989802
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1569355102
rs1569355102
T 0.700 CausalMutation CLINVAR

dbSNP: rs376103091
rs376103091
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519521
rs1057519521
T 0.700 CausalMutation CLINVAR