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: rs3024493
rs3024493
9 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.720 1.000 4 2013 2019
dbSNP: rs1800896
rs1800896
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 0.667 3 2018 2019
dbSNP: rs1518110
rs1518110
5 0.851 0.160 1 206771516 intron variant A/C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs1518111
rs1518111
9 0.790 0.360 1 206771300 intron variant T/C snv 0.71 0.010 1.000 1 2018 2018
dbSNP: rs1800871
rs1800871
108 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.010 1.000 1 2019 2019
dbSNP: rs1800872
rs1800872
119 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2019 2019
dbSNP: rs3024495
rs3024495
1 1.000 0.080 1 206769068 intron variant C/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs3024498
rs3024498
7 0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 0.010 1.000 1 2018 2018