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: rs7193263
rs7193263
1 1.000 0.040 16 6265879 intron variant G/A snv 0.52 0.700 1.000 2 2018 2019
dbSNP: rs7198928
rs7198928
1 1.000 0.040 16 7616400 intron variant T/A;C snv 0.700 1.000 2 2018 2019
dbSNP: rs2191130
rs2191130
1 1.000 0.040 16 7617795 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs3785234
rs3785234
1 1.000 0.040 16 7617390 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs3785236
rs3785236
1 1.000 0.040 16 7617197 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs8063603
rs8063603
1 1.000 0.040 16 6260644 intron variant G/A snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs9930139
rs9930139
2 1.000 0.040 16 7239569 intron variant A/C;T snv 0.700 1.000 1 2018 2018