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: rs1260326
rs1260326
63 0.667 0.321 2 27508073 missense variant T/C snp 0.63; 4.0E-06 0.67 0.800 2 2012 2016
dbSNP: rs4273077
rs4273077
2 1.000 0.143 17 16945825 intron variant A/G snp 0.14 0.800 2 2010 2012
dbSNP: rs1990760
rs1990760
16 0.744 0.286 2 162267541 missense variant C/T snp 0.50 0.46 0.800 1 2010 2010
dbSNP: rs2187668
rs2187668
15 0.724 0.393 6 32638107 intron variant C/T snp 0.800 1 2010 2010
dbSNP: rs2274273
rs2274273
1 14 55147918 intergenic variant G/A snp 0.41 0.800 1 2012 2012
dbSNP: rs4985726
rs4985726
1 17 16960324 intron variant C/G snp 0.12 0.800 1 2012 2012
dbSNP: rs644234
rs644234
8 1.000 0.036 None NA snp 0.42 0.800 1 2012 2012
dbSNP: rs6498142
rs6498142
2 16 10987392 intron variant C/G snp 0.78 0.800 1 2010 2010
dbSNP: rs9271366
rs9271366
8 0.801 0.214 6 32619077 intergenic variant G/A snp 0.800 1 2010 2010
dbSNP: rs10007186
rs10007186
1 4 78667891 intron variant C/T snp 3.2E-05; 0.65 0.700 1 2012 2012
dbSNP: rs1002054
rs1002054
1 14 55062195 intron variant A/C,T snp 0.52 0.700 1 2012 2012
dbSNP: rs10083777
rs10083777
2 16 81031677 intron variant C/T snp 0.16 0.700 1 2016 2016
dbSNP: rs1009647
rs1009647
2 1.000 0.107 14 55413329 intergenic variant G/A snp 0.25 0.700 1 2012 2012
dbSNP: rs1009648
rs1009648
1 14 55413451 intergenic variant T/C snp 0.29 0.700 1 2012 2012
dbSNP: rs1009714
rs1009714
1 14 55512820 intron variant A/G,T snp 0.55 0.700 1 2012 2012
dbSNP: rs1009977
rs1009977
1 14 55136284 intron variant T/G snp 0.49 0.700 1 2012 2012
dbSNP: rs1009978
rs1009978
1 14 55136343 intron variant C/G,T snp 0.56 0.700 1 2012 2012
dbSNP: rs10129505
rs10129505
1 14 55309657 intron variant C/T snp 0.32 0.700 1 2012 2012
dbSNP: rs10130783
rs10130783
1 14 55714800 intergenic variant G/A snp 0.24 0.700 1 2012 2012
dbSNP: rs10131232
rs10131232
1 14 54849190 intron variant G/A snp 0.46 0.700 1 2012 2012
dbSNP: rs10131730
rs10131730
1 14 55373374 intron variant C/T snp 0.32 0.700 1 2012 2012
dbSNP: rs10133662
rs10133662
1 14 54849552 intron variant A/G snp 0.46 0.700 1 2012 2012
dbSNP: rs10134019
rs10134019
1 14 55530274 intron variant T/G snp 0.55 0.700 1 2012 2012
dbSNP: rs10134317
rs10134317
1 14 55326730 intron variant C/A,G,T snp 0.33 0.700 1 2012 2012
dbSNP: rs10134339
rs10134339
1 14 55347662 intron variant T/C snp 0.57 0.700 1 2012 2012