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: rs2078486
rs2078486
3 0.882 0.080 17 7679765 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs78378222
rs78378222
22 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 0.010 1.000 1 2013 2013
dbSNP: rs1800371
rs1800371
15 0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 0.010 1.000 1 2014 2014
dbSNP: rs587782596
rs587782596
5 0.807 0.200 17 7675071 missense variant G/A;T snv 0.010 1.000 1 2017 2017
dbSNP: rs121912654
rs121912654
19 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 0.010 1.000 1 2020 2020
dbSNP: rs483352697
rs483352697
3 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2020 2020