Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs797045045
rs797045045
GABRB3
2 1.000 15 26567721 missense variant C/G;T snv 0.700 1.000 2 2016 2017
dbSNP: rs1057519201
rs1057519201
GABRB3
2 1.000 15 26621395 missense variant T/C snv 0.700 1.000 1 2017 2017
dbSNP: rs1555401942
rs1555401942
GABRB3
1 15 26567650 missense variant G/C snv 0.700 0
dbSNP: rs1567106381
rs1567106381
GABRB3
2 1.000 15 26561117 missense variant T/G snv 0.700 0
dbSNP: rs25409
rs25409
GABRB3 ; LOC112268151
4 0.882 0.080 15 26773694 missense variant G/A snv 2.9E-03 3.5E-03 0.700 0
dbSNP: rs71651682
rs71651682
GABRB3 ; LOC112268151
3 0.925 0.040 15 26772759 missense variant C/T snv 0.700 0