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: rs1135642
rs1135642
1 4 77031856 3 prime UTR variant G/A snv 7.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs12126348
rs12126348
1 1 192065896 intergenic variant G/T snv 1.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs139878170
rs139878170
1 6 126699724 intron variant C/A snv 2.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs147346874
rs147346874
1 5 7296610 intron variant A/G snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs74902201
rs74902201
1 17 66715445 intron variant G/A snv 5.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs75038630
rs75038630
1 11 131888434 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs8073426
rs8073426
1 17 65567163 intron variant T/C snv 0.62 0.700 1.000 1 2018 2018