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: rs10919388
rs10919388
4 1 170403362 intergenic variant A/C snv 0.71 0.700 1.000 3 2018 2019
dbSNP: rs7823561
rs7823561
1 8 25784248 intergenic variant A/C snv 0.38 0.700 1.000 3 2018 2019
dbSNP: rs11726981
rs11726981
1 4 124299553 intergenic variant A/C snv 0.30 0.700 1.000 2 2018 2019
dbSNP: rs39312
rs39312
1 7 117314731 intron variant A/C snv 0.43 0.700 1.000 2 2018 2019
dbSNP: rs10512606
rs10512606
1 17 76215127 intron variant A/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs10843817
rs10843817
1 12 30712576 intron variant A/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs10844642
rs10844642
1 12 33577433 downstream gene variant A/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs11247113
rs11247113
1 15 99577110 intron variant A/C snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs11592754
rs11592754
1 10 32330644 intron variant A/C snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs13406302
rs13406302
1 2 37647707 intron variant A/C snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs144033177
rs144033177
1 20 590823 intergenic variant A/C snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs1568799
rs1568799
1 7 42628277 intergenic variant A/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs270960
rs270960
1 2 160858218 intergenic variant A/C snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs35915890
rs35915890
1 7 14188819 intron variant A/C snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs4536164
rs4536164
1 11 27445562 intron variant A/C snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs4681011
rs4681011
1 3 78786588 intron variant A/C snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs4686340
rs4686340
2 3 9303534 intron variant A/C snv 0.80 0.700 1.000 1 2019 2019
dbSNP: rs6090040
rs6090040
2 20 64060707 intron variant A/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs62506196
rs62506196
1 8 59351906 intergenic variant A/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs6428789
rs6428789
1 1 119007857 regulatory region variant A/C snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs6727396
rs6727396
1 2 134741666 intron variant A/C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs6795831
rs6795831
1 3 129622560 intergenic variant A/C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs68162171
rs68162171
1 11 66357990 intron variant A/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs758801
rs758801
2 1.000 0.040 3 52502292 intron variant A/C snv 0.86 0.700 1.000 1 2019 2019
dbSNP: rs762705
rs762705
2 3 50276096 non coding transcript exon variant A/C snv 0.700 1.000 1 2019 2019