Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3752651 1.000 0.040 7 55161850 intron variant T/C snv 0.15 1
rs6958497 1.000 0.080 7 55094053 intron variant T/C snv 0.14 1
rs2293347 0.851 0.080 7 55201223 synonymous variant C/T snv 0.14 9.5E-02 4
rs759165 1.000 0.080 7 55049014 intron variant G/A snv 4.3E-02 1
rs17172445 1.000 0.040 7 55121522 intron variant G/T snv 2.2E-02 1
rs17290301 1.000 0.040 7 55173189 intron variant G/A snv 2.0E-02 1
rs114972508 0.925 0.120 7 55020815 intron variant T/C snv 1.4E-02 2
rs35918369 7 55205613 missense variant C/T snv 3.1E-04 3.3E-04 4
rs150423237 7 55173087 missense variant G/A snv 2.1E-04 2.4E-04 1
rs140516819 7 55172999 missense variant A/C;G snv 4.0E-05 2.4E-04 4
rs371228501 1.000 0.040 7 55191740 missense variant C/T snv 6.8E-05 1.2E-04 1
rs376822837 1.000 0.080 7 55198761 missense variant G/A snv 3.6E-05 6.3E-05 1
rs533525993 1.000 0.040 7 55165435 splice region variant C/T snv 2.4E-04 5.6E-05 1
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs150036236 0.925 0.080 7 55191741 missense variant G/A snv 4.8E-05 3.5E-05 3
rs778985185 0.851 0.160 7 55163734 missense variant G/A snv 8.0E-06 3.5E-05 5
rs377444977 0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs760101437 0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 6
rs758748662 1.000 0.160 7 55155911 missense variant G/A snv 4.0E-06 1.4E-05 1
rs754426793 0.925 0.080 7 55181395 missense variant G/A snv 1.2E-05 1.4E-05 2
rs780439043 0.925 0.080 7 55205301 missense variant A/G snv 8.0E-06 1.4E-05 3
rs759106015 7 55152588 missense variant G/A snv 3.2E-05 1.4E-05 1
rs764290273 1.000 0.040 7 55165394 missense variant G/A snv 8.0E-06 1.4E-05 1
rs771398183 1.000 0.040 7 55156554 missense variant G/T snv 4.0E-06 1.4E-05 1
rs767505234 1.000 0.040 7 55174033 missense variant C/T snv 1.4E-05 3