Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 2
rs1511237 1.000 0.040 11 79403640 intron variant C/T snv 0.11 1
rs1944449 1.000 0.040 11 79372205 intron variant C/T snv 0.18 1
rs11237799 1.000 0.040 11 79356427 intron variant A/C;T snv 1
rs10501439 1.000 0.040 11 79374802 intron variant A/G snv 0.18 1
rs11237815 1.000 0.040 11 79379756 intron variant A/G snv 0.10 1
rs12577328 1.000 0.040 11 79382430 intron variant C/G snv 8.3E-02 1
rs11237821 1.000 0.040 11 79395760 intron variant C/A;T snv 1
rs12577093 1.000 0.040 11 79346052 intron variant C/A;T snv 1
rs7108878 1.000 0.040 11 79396763 intron variant T/G snv 0.10 1
rs17138230 0.925 0.080 11 79364808 intron variant A/T snv 0.16 1
rs11237805 1.000 0.040 11 79367625 intron variant A/G;T snv 1
rs12275195 1.000 0.040 11 79394755 intron variant A/C snv 0.12 1
rs12290811 0.882 0.120 11 79372576 intron variant T/A snv 0.18 1
rs12277834 1.000 0.040 11 79389112 intron variant C/A;T snv 1
rs17138171 1.000 0.040 11 79351885 intron variant T/A;C snv 1
rs7127580 1.000 0.040 11 79433812 intron variant C/A;G snv 1
rs12289486 1.000 0.040 11 79381483 intron variant C/T snv 8.4E-02 1
rs11237796 1.000 0.040 11 79348399 intron variant A/G snv 0.16 1
rs954129 1.000 0.040 11 79349751 intron variant T/A snv 0.18 1
rs12279388 1.000 0.040 11 79356629 intron variant A/G snv 0.15 1
rs11237820 1.000 0.040 11 79393621 intron variant G/A snv 8.7E-02 1
rs7932890 0.925 0.080 11 79357349 intron variant A/G snv 0.19 1
rs499949 11 79282162 intron variant C/T snv 0.58 1
rs1151200 11 79281641 intron variant T/C snv 0.50 1