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: rs1036467
rs1036467
ABI3BP
1 3 100923960 intron variant C/T snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs10511181
rs10511181
ABI3BP
1 3 100971018 intron variant T/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs13060137
rs13060137
ABI3BP
1 3 100929083 intron variant A/G snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs13072000
rs13072000
ABI3BP
1 3 100906978 intron variant A/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs13074729
rs13074729 		1 3 101046740 intergenic variant G/T snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs13077353
rs13077353
ABI3BP
1 3 100931463 intron variant T/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs13079002
rs13079002
ABI3BP
1 3 100911297 non coding transcript exon variant C/T snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs13081830
rs13081830 		1 3 101072418 TF binding site variant G/A snv 9.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs13088524
rs13088524
ABI3BP
1 3 100969238 intron variant A/C snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs13099753
rs13099753 		1 3 101050480 regulatory region variant C/G snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs16843216
rs16843216 		1 3 101078035 intergenic variant C/T snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs16843225
rs16843225 		1 3 101082413 regulatory region variant T/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs16843229
rs16843229 		1 3 101083376 intergenic variant G/A snv 0.18 0.700 1.000 1 2010 2010
dbSNP: rs17219986
rs17219986 		1 3 101080826 intergenic variant G/A snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs17284842
rs17284842
ABI3BP
1 3 100926103 intron variant T/C snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs17398421
rs17398421
ABI3BP
1 3 100954063 intron variant T/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs17398684
rs17398684
ABI3BP
1 3 100976498 intron variant G/A snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs17399603
rs17399603 		2 1.000 0.040 3 101017295 regulatory region variant A/G snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs2245266
rs2245266
ABI3BP
1 3 100899929 intron variant T/C snv 0.83 0.700 1.000 1 2010 2010
dbSNP: rs2245473
rs2245473
ABI3BP
1 3 100897292 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs2245556
rs2245556
ABI3BP
1 3 100896706 intron variant T/C snv 0.83 0.700 1.000 1 2010 2010
dbSNP: rs2576365
rs2576365
ABI3BP
1 3 100902582 intron variant C/A;G snv 0.88 0.83 0.700 1.000 1 2010 2010
dbSNP: rs2576369
rs2576369
ABI3BP
1 3 100899311 intron variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2576377
rs2576377
ABI3BP
1 3 100928905 intron variant C/T snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs2576382
rs2576382
ABI3BP
1 3 100948985 intron variant T/A snv 0.86 0.700 1.000 1 2010 2010