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: rs1190982
rs1190982
1 14 58349121 intron variant T/C snv 0.68 0.700 1.000 3 2018 2019
dbSNP: rs12774134
rs12774134
1 10 4921135 intergenic variant C/T snv 0.11 0.700 1.000 3 2018 2019
dbSNP: rs1294410
rs1294410
3 6 6738519 intron variant T/C snv 0.65 0.800 1.000 3 2013 2019
dbSNP: rs13028903
rs13028903
1 2 59724330 intron variant C/T snv 0.41 0.700 1.000 3 2018 2019
dbSNP: rs1328757
rs1328757
1 20 57560143 upstream gene variant C/T snv 0.41 0.700 1.000 3 2018 2019
dbSNP: rs1358980
rs1358980
6 6 43796814 intergenic variant C/T snv 0.40 0.700 1.000 3 2013 2019
dbSNP: rs1440372
rs1440372
1 15 66740813 non coding transcript exon variant T/C snv 0.78 0.700 1.000 3 2015 2019
dbSNP: rs1443512
rs1443512
4 12 53948900 downstream gene variant A/C;T snv 0.800 1.000 3 2010 2018
dbSNP: rs1569135
rs1569135
3 2 187250671 intron variant A/G snv 0.51 0.700 1.000 3 2015 2019
dbSNP: rs17326656
rs17326656
1 2 48735152 intron variant G/T snv 0.21 0.700 1.000 3 2018 2019
dbSNP: rs2167750
rs2167750
1 4 88808923 intron variant C/T snv 0.50 0.700 1.000 3 2018 2019
dbSNP: rs2294239
rs2294239
4 22 29053489 intron variant A/G snv 0.36 0.700 1.000 3 2018 2019
dbSNP: rs2398893
rs2398893
1 9 93996060 intergenic variant A/G snv 0.31 0.700 1.000 3 2015 2019
dbSNP: rs332105
rs332105
1 2 118686653 regulatory region variant G/A snv 0.57 0.700 1.000 3 2018 2019
dbSNP: rs577721086
rs577721086
1 6 127118902 splice region variant T/C snv 3.3E-02 0.700 1.000 3 2017 2019
dbSNP: rs7823561
rs7823561
1 8 25784248 intergenic variant A/C snv 0.38 0.700 1.000 3 2018 2019
dbSNP: rs905938
rs905938
5 1 155018913 intron variant T/C snv 0.24 0.700 1.000 3 2018 2019
dbSNP: rs998584
rs998584
11 6 43790159 downstream gene variant C/A snv 0.41 0.700 1.000 3 2018 2019
dbSNP: rs1011731
rs1011731
4 1 172377408 intron variant G/A snv 0.46 0.800 1.000 2 2010 2015
dbSNP: rs10477191
rs10477191
1 5 142698150 upstream gene variant A/G snv 0.22 0.700 1.000 2 2019 2019
dbSNP: rs1053593
rs1053593
2 22 35264882 missense variant G/C;T snv 8.0E-06; 0.58 0.700 1.000 2 2018 2019
dbSNP: rs10745659
rs10745659
1 12 93698914 intron variant C/A;G snv 0.700 1.000 2 2018 2019
dbSNP: rs10795055
rs10795055
1 10 3539029 intron variant A/G snv 0.54 0.700 1.000 2 2019 2019
dbSNP: rs10923724
rs10923724
3 1 119004219 upstream gene variant C/T snv 0.53 0.700 1.000 2 2018 2019