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: rs13390936
rs13390936
3 0.925 0.080 2 191090090 intron variant A/T snv 8.4E-02 0.010 1.000 1 2018 2018
dbSNP: rs1800795
rs1800795
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.010 1.000 1 2015 2015
dbSNP: rs7633054
rs7633054
1 1.000 0.080 3 62153280 intron variant C/G snv 4.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs926632
rs926632
3 0.882 0.160 20 59309707 intron variant C/T snv 0.61 0.010 1.000 1 2019 2019
dbSNP: rs4694744
rs4694744
1 1.000 0.080 4 69460938 intergenic variant T/C snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs5744168
rs5744168
18 0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 0.020 1.000 2 2015 2017
dbSNP: rs1799983
rs1799983
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2009 2009