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: rs1713222
rs1713222
3 2 21048451 upstream gene variant A/G snv 0.82 0.700 1.000 1 2008 2008
dbSNP: rs2254287
rs2254287
3 1.000 0.040 6 33176171 intron variant C/A;G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs4560142
rs4560142
2 2 21160845 intergenic variant C/T snv 0.75 0.700 1.000 1 2008 2008
dbSNP: rs4591370
rs4591370
3 2 21160870 intergenic variant A/G snv 0.75 0.700 1.000 1 2008 2008
dbSNP: rs4605275
rs4605275
3 1.000 0.080 19 44835236 intergenic variant T/C snv 0.69 0.700 1.000 1 2008 2008
dbSNP: rs478442
rs478442
18 0.851 0.120 2 21176344 intergenic variant G/C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs488507
rs488507
2 2 21170817 intergenic variant G/T snv 0.78 0.700 1.000 1 2008 2008
dbSNP: rs506585
rs506585
4 2 21174310 intergenic variant G/A;C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs538928
rs538928
2 2 21166147 intergenic variant A/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs576203
rs576203
2 2 21170751 intergenic variant A/G snv 0.76 0.700 1.000 1 2008 2008
dbSNP: rs6589566
rs6589566
10 0.882 0.080 11 116781707 intron variant G/A;C;T snv 0.700 1.000 1 2008 2008
dbSNP: rs7703051
rs7703051
18 0.851 0.120 5 75329662 intron variant C/A snv 0.38 0.700 1.000 1 2008 2008
dbSNP: rs780094
rs780094
62 0.658 0.400 2 27518370 intron variant T/C snv 0.67 0.700 1.000 1 2008 2008
dbSNP: rs11668477
rs11668477
7 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 0.700 1.000 2 2008 2009
dbSNP: rs1501908
rs1501908
5 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs174570
rs174570
11 0.882 0.200 11 61829740 intron variant C/T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs2650000
rs2650000
10 0.851 0.200 12 120951159 intron variant A/C snv 0.70 0.700 1.000 1 2009 2009
dbSNP: rs3846663
rs3846663
7 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.700 1.000 1 2009 2009
dbSNP: rs4844614
rs4844614
3 1.000 0.040 1 207701830 intron variant G/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs5031002
rs5031002
AR
3 1.000 0.040 X 67722783 intron variant G/A snv 1.5E-02 1.5E-02 0.700 1.000 1 2009 2009
dbSNP: rs6102059
rs6102059
3 1.000 0.040 20 40600144 intergenic variant C/T snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs6756629
rs6756629
5 0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 0.700 1.000 1 2009 2009
dbSNP: rs2126259
rs2126259
9 1.000 8 9327636 intron variant T/C snv 0.87 0.700 1.000 1 2010 2010
dbSNP: rs2142672
rs2142672
2 6 16196963 intergenic variant G/A snv 0.42 0.700 1.000 1 2010 2010
dbSNP: rs2954021
rs2954021
15 1.000 0.040 8 125469835 intron variant A/G snv 0.54 0.700 1.000 1 2010 2010