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: rs10462706
rs10462706
6 0.827 0.080 5 1343679 intron variant C/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs10851478
rs10851478
6 0.827 0.080 15 49536822 intron variant T/C snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs1229984
rs1229984
83 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.700 1.000 1 2016 2016
dbSNP: rs1453414
rs1453414
7 0.827 0.080 11 5807854 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1800628
rs1800628
6 0.827 0.080 6 31579073 downstream gene variant G/A snv 7.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs2398180
rs2398180
6 0.827 0.080 15 96319940 intron variant C/T snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs3129780
rs3129780
6 0.827 0.080 6 32679924 intergenic variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs3828805
rs3828805
12 0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs6547741
rs6547741
7 0.807 0.080 2 27633057 intron variant G/A snv 0.53 0.700 1.000 1 2016 2016
dbSNP: rs77452476
rs77452476
7 0.827 0.080 9 131087186 intron variant T/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs79767424
rs79767424
7 0.827 0.080 5 19108581 intron variant G/T snv 4.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs8181047
rs8181047
7 0.807 0.120 9 22064466 intron variant A/G snv 0.79 0.700 1.000 1 2016 2016
dbSNP: rs928674
rs928674
6 0.827 0.080 9 131076637 intron variant A/G snv 0.16 0.700 1.000 1 2016 2016