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: rs2150127
rs2150127
1 13 93838807 intron variant A/G snv 7.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs2245266
rs2245266
1 3 100899929 intron variant T/C snv 0.83 0.700 1.000 1 2010 2010
dbSNP: rs2245473
rs2245473
1 3 100897292 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs2245556
rs2245556
1 3 100896706 intron variant T/C snv 0.83 0.700 1.000 1 2010 2010
dbSNP: rs2576365
rs2576365
1 3 100902582 intron variant C/A;G snv 0.88 0.83 0.700 1.000 1 2010 2010
dbSNP: rs2576369
rs2576369
1 3 100899311 intron variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2576377
rs2576377
1 3 100928905 intron variant C/T snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs2576382
rs2576382
1 3 100948985 intron variant T/A snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs2576391
rs2576391
1 3 100958166 intron variant C/G snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs2595893
rs2595893
1 3 100958998 intron variant C/T snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs2595894
rs2595894
1 3 100959038 intron variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2602098
rs2602098
1 4 71269738 intron variant T/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs2713782
rs2713782
1 3 100910460 intron variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2713787
rs2713787
1 3 100905594 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs2713793
rs2713793
1 3 100900330 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs384005
rs384005
2 5 88709286 intron variant T/C snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs4053798
rs4053798
1 6 85233471 intergenic variant A/C snv 1.00 0.700 1.000 1 2018 2018
dbSNP: rs4060963
rs4060963
1 3 100905717 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs4554696
rs4554696
2 1 65942328 intron variant C/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs4809706
rs4809706
1 20 48577181 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4928096
rs4928096
1 3 100900916 intron variant G/A snv 0.85 0.700 1.000 1 2010 2010
dbSNP: rs61606793
rs61606793
1 3 178690059 intron variant T/G snv 7.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs62199592
rs62199592
2 2 183858773 intergenic variant A/G snv 2.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs6475417
rs6475417
2 9 20212043 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6661750
rs6661750
2 1 66081201 intron variant A/G;T snv 0.700 1.000 1 2018 2018