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: rs10911268
rs10911268
1 1.000 0.040 1 183153583 intergenic variant C/A snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs1092479
rs1092479
1 1.000 0.040 2 121011861 intergenic variant G/C snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs11118336
rs11118336
1 1.000 0.040 1 219547941 intergenic variant C/T snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs1159268
rs1159268
1 1.000 0.040 1 218671564 regulatory region variant G/A snv 0.32 0.700 1.000 1 2014 2014
dbSNP: rs121908120
rs121908120
19 0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs1256580
rs1256580
1 1.000 0.040 1 219026038 intron variant G/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs144991069
rs144991069
1 1.000 0.040 11 65060236 upstream gene variant T/A snv 6.8E-03 0.700 1.000 1 2018 2018
dbSNP: rs1533326
rs1533326
1 1.000 0.040 15 90211722 intron variant A/G snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs158639
rs158639
1 1.000 0.040 5 56315883 intron variant G/A snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs17651189
rs17651189
1 1.000 0.040 22 24448915 intron variant T/C snv 2.9E-02 0.700 1.000 1 2014 2014
dbSNP: rs2242095
rs2242095
1 1.000 0.040 8 143596704 5 prime UTR variant C/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs2727365
rs2727365
1 1.000 0.040 11 13089937 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs28360612
rs28360612
1 1.000 0.040 22 24487250 intron variant T/A snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs28405582
rs28405582
1 1.000 0.040 3 23863271 intron variant T/C snv 4.6E-02 0.700 1.000 1 2014 2014
dbSNP: rs28570522
rs28570522
1 1.000 0.040 8 10773058 intron variant A/G snv 0.66 0.700 1.000 1 2018 2018
dbSNP: rs2901000
rs2901000
1 1.000 0.040 2 60274081 intergenic variant A/G snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs330071
rs330071
1 1.000 0.040 8 9302385 intron variant G/A snv 0.25 0.700 1.000 1 2014 2014
dbSNP: rs34560261
rs34560261
3 0.882 0.040 15 90191194 intron variant C/T snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs38055
rs38055
1 1.000 0.040 5 53264814 intergenic variant A/G snv 0.75 0.700 1.000 1 2014 2014
dbSNP: rs4487353
rs4487353
1 1.000 0.040 4 123332634 intergenic variant G/A snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs478304
rs478304
1 1.000 0.040 11 65726789 upstream gene variant G/T snv 0.54 0.700 1.000 1 2014 2014
dbSNP: rs61744384
rs61744384
1 1.000 0.040 11 65619907 synonymous variant T/A;G snv 0.45; 4.1E-06 0.700 1.000 1 2018 2018
dbSNP: rs629725
rs629725
1 1.000 0.040 5 53335237 TF binding site variant T/C snv 0.74 0.700 1.000 1 2018 2018
dbSNP: rs6684868
rs6684868
1 1.000 0.040 1 218674648 TF binding site variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs72966077
rs72966077
1 1.000 0.040 2 218894507 intron variant C/T snv 3.3E-02 0.700 1.000 1 2018 2018