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: rs1801133
rs1801133
174 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 0.700 1.000 2 2018 2018
dbSNP: rs11194787
rs11194787
1 10 109674583 intergenic variant G/A snv 1.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs12611820
rs12611820
1 2 2479854 intergenic variant T/G snv 0.33 0.700 1.000 1 2014 2014
dbSNP: rs17393539
rs17393539
1 7 31301873 intergenic variant T/A snv 6.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs1999594
rs1999594
2 1 11899159 regulatory region variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2639453
rs2639453
2 1 11922487 3 prime UTR variant T/C snv 0.77 0.81 0.700 1.000 1 2018 2018
dbSNP: rs2670029
rs2670029
1 8 56472437 intron variant C/A snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs3782886
rs3782886
22 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 0.700 1.000 1 2018 2018