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: rs587777771
rs587777771
ATP1A3
4 0.851 0.240 19 41970275 missense variant C/T snv 0.870 1.000 8 2014 2019
dbSNP: rs1064797245
rs1064797245
ATP1A3
12 0.776 0.280 19 41970540 missense variant G/A snv 0.710 1.000 5 2015 2018
dbSNP: rs1135401821
rs1135401821
ATP1A3
1 1.000 0.240 19 41986127 missense variant T/C snv 0.700 0
dbSNP: rs1135401822
rs1135401822
ATP1A3
1 1.000 0.240 19 41975668 missense variant C/A snv 0.700 0
dbSNP: rs267606670
rs267606670
ATP1A3
19 0.790 0.320 19 41968837 missense variant C/A;T snv 0.700 0
dbSNP: rs387907281
rs387907281
ATP1A3
13 0.752 0.280 19 41970284 missense variant C/T snv 0.700 0
dbSNP: rs398122887
rs398122887
ATP1A3
8 0.790 0.280 19 41967744 missense variant C/G;T snv 0.700 0
dbSNP: rs606231435
rs606231435
ATP1A3
18 0.827 0.240 19 41970539 missense variant C/T snv 0.700 0
dbSNP: rs80356537
rs80356537
ATP1A3
17 0.752 0.320 19 41970405 missense variant C/A;G;T snv 0.700 0
dbSNP: rs863224847
rs863224847
ATP1A3
1 1.000 0.240 19 41984937 missense variant C/T snv 0.700 0
dbSNP: rs782503624
rs782503624
ATP1A3
2 0.925 0.240 19 41970308 missense variant C/T snv 4.0E-06 0.040 1.000 4 2015 2019