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: rs752746786
rs752746786
GNB1
30 0.742 0.560 1 1806503 missense variant A/C;G;T snv 4.0E-06 0.800 1.000 4 2015 2017
dbSNP: rs869312825
rs869312825
GNB1
11 0.827 0.120 1 1804548 start lost T/C snv 0.800 1.000 4 2015 2017
dbSNP: rs869312821
rs869312821
GNB1
7 0.882 0.120 1 1806515 missense variant T/C snv 0.800 0
dbSNP: rs869312823
rs869312823
GNB1
9 0.882 0.080 1 1806509 missense variant T/C snv 0.800 0
dbSNP: rs1553194162
rs1553194162
GNB1
2 1.000 1 1804496 missense variant T/C snv 0.700 1.000 4 2015 2017
dbSNP: rs869312824
rs869312824
GNB1
14 0.827 0.200 1 1804565 missense variant A/G snv 0.700 1.000 4 2015 2017
dbSNP: rs869312826
rs869312826
GNB1
6 0.882 0.080 1 1787378 missense variant C/T snv 0.700 1.000 4 2015 2017
dbSNP: rs1557898800
rs1557898800
GNB1
1 1.000 1 1815801 missense variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs1135401746
rs1135401746
GNB1
7 0.827 0.400 1 1806512 missense variant C/G snv 0.700 0
dbSNP: rs758432471
rs758432471
GNB1
4 0.925 1 1806513 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs764997309
rs764997309
GNB1
1 1.000 1 1817845 missense variant G/A snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs869312822
rs869312822
GNB1
8 0.827 0.200 1 1806514 missense variant A/C snv 0.700 0