Source: ALL
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: rs11176001
rs11176001 		3 12 66015587 regulatory region variant C/A snv 9.6E-02 0.700 1.000 2 2019 2019
dbSNP: rs1192415
rs1192415 		4 0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81 0.700 1.000 2 2019 2019
dbSNP: rs12497779
rs12497779 		2 3 99103206 intergenic variant G/T snv 0.25 0.700 1.000 2 2019 2019
dbSNP: rs12698403
rs12698403 		3 7 156334552 intergenic variant G/A snv 0.40 0.700 1.000 2 2019 2019
dbSNP: rs17009288
rs17009288 		2 1 221030957 regulatory region variant A/C snv 0.30 0.700 1.000 2 2019 2019
dbSNP: rs35043843
rs35043843 		3 1 118368672 intergenic variant T/G snv 0.21 0.700 1.000 2 2019 2019
dbSNP: rs4952564
rs4952564 		2 2 42016710 intron variant A/G snv 0.43 0.700 1.000 2 2019 2019
dbSNP: rs6501431
rs6501431 		1 17 70980274 intergenic variant C/T snv 0.81 0.700 1.000 2 2014 2019
dbSNP: rs91731
rs91731 		1 5 33334206 intergenic variant C/A;T snv 0.700 1.000 2 2017 2019
dbSNP: rs9357446
rs9357446 		2 6 44479861 intergenic variant G/A snv 0.64 0.700 1.000 2 2019 2019
dbSNP: rs9689096
rs9689096 		2 6 34221115 downstream gene variant A/C snv 0.11 0.700 1.000 2 2019 2019
dbSNP: rs10005540
rs10005540 		1 4 173660916 downstream gene variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1000972
rs1000972 		2 20 6641070 regulatory region variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10041818
rs10041818 		1 5 148691691 intergenic variant C/T snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs10088136
rs10088136 		1 8 85482363 downstream gene variant T/A snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs10089933
rs10089933 		1 8 48478923 intergenic variant T/C snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs10136987
rs10136987 		1 14 93842954 intergenic variant G/A snv 0.89 0.700 1.000 1 2019 2019
dbSNP: rs10201883
rs10201883 		1 2 177606679 intron variant T/C snv 0.82 0.700 1.000 1 2019 2019
dbSNP: rs10214145
rs10214145 		1 5 27636685 intergenic variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1035101
rs1035101 		1 2 59563217 intron variant C/T snv 0.60 0.700 1.000 1 2019 2019
dbSNP: rs1041733
rs1041733 		1 21 34311960 intron variant T/A snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs1074765
rs1074765 		2 6 109360458 intergenic variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs1074993
rs1074993 		1 12 12281304 regulatory region variant A/G snv 0.75 0.700 1.000 1 2019 2019
dbSNP: rs10779447
rs10779447 		1 1 221587993 intergenic variant A/G snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs1080278
rs1080278 		1 2 209410985 intergenic variant G/A snv 0.22 0.700 1.000 1 2019 2019