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: rs10830963
rs10830963
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.700 1.000 3 2016 2019
dbSNP: rs10935733
rs10935733
1 3 148905181 intron variant T/C snv 0.52 0.700 1.000 2 2016 2019
dbSNP: rs11096402
rs11096402
1 X 134693838 intron variant G/A snv 0.52 0.700 1.000 2 2016 2019
dbSNP: rs13266210
rs13266210
1 8 41675996 intron variant A/G snv 0.21 0.700 1.000 2 2016 2019
dbSNP: rs13322435
rs13322435
3 3 157077679 upstream gene variant A/G snv 0.46 0.700 1.000 2 2016 2019
dbSNP: rs134594
rs134594
1 22 29072468 upstream gene variant C/T snv 0.65 0.700 1.000 2 2016 2019
dbSNP: rs138715366
rs138715366
1 7 44206672 intron variant C/T snv 5.9E-03 0.700 1.000 2 2016 2019
dbSNP: rs1415701
rs1415701
3 6 130024690 intron variant G/A snv 0.31 0.700 1.000 2 2016 2019
dbSNP: rs2229742
rs2229742
3 21 14966851 missense variant G/C snv 7.9E-02 7.1E-02 0.700 1.000 2 2016 2019
dbSNP: rs2242116
rs2242116
1 3 46899626 intron variant A/G snv 0.53 0.700 1.000 2 2016 2019
dbSNP: rs2971669
rs2971669
GCK
1 7 44192179 intron variant C/T snv 0.30 0.700 1.000 2 2018 2019
dbSNP: rs35261542
rs35261542
3 1.000 0.080 6 20675561 intron variant C/A snv 0.26 0.700 1.000 2 2016 2019
dbSNP: rs6040076
rs6040076
1 20 10678234 intron variant G/A;C snv 0.700 1.000 2 2016 2019
dbSNP: rs61830764
rs61830764
1 1 212116634 intergenic variant G/A snv 0.28 0.700 1.000 2 2016 2019
dbSNP: rs7076938
rs7076938
3 10 114029616 intergenic variant C/T snv 0.69 0.700 1.000 2 2016 2019
dbSNP: rs72480273
rs72480273
1 1 161675081 non coding transcript exon variant A/C snv 0.16 0.700 1.000 2 2016 2019
dbSNP: rs854037
rs854037
1 5 57795956 intergenic variant A/G snv 0.30 0.700 1.000 2 2016 2019
dbSNP: rs9379832
rs9379832
3 1.000 0.080 6 26185972 downstream gene variant A/G snv 0.26 0.700 1.000 2 2016 2019
dbSNP: rs1011939
rs1011939
1 16 19981674 intergenic variant G/A snv 0.59 0.700 1.000 1 2016 2016
dbSNP: rs1012167
rs1012167
1 20 40530479 intergenic variant T/C snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs10147938
rs10147938
1 14 31416745 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs10173538
rs10173538
5 2 159712765 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10181515
rs10181515
1 2 226154745 TF binding site variant C/T snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs10221267
rs10221267
1 17 70468521 intergenic variant C/T snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs10265057
rs10265057
1 7 47236139 intergenic variant A/G snv 0.15 0.700 1.000 1 2019 2019