Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs669676 1.000 0.040 3 99730008 intron variant A/G snv 0.45 2
rs79002828 0.925 0.040 5 44318015 intron variant A/G snv 9.6E-03 2
rs9747347 1.000 0.040 17 81639794 intron variant T/A;C;G snv 2
rs9866391 1.000 0.040 3 141357242 intron variant T/C snv 0.41 2
rs10462070 1.000 0.040 5 44305647 intron variant A/G snv 1.2E-02 1
rs10511652 1.000 0.040 9 18362867 intron variant A/G snv 0.54 1
rs10887265
RGR
1.000 0.040 10 84255817 intron variant G/C snv 0.48 1
rs11145488 1.000 0.040 9 69156023 intron variant G/A snv 0.19 1
rs11218544 1.000 0.040 11 122168344 intron variant T/G snv 0.15 1
rs11606250 1.000 0.040 11 40127750 intron variant G/A snv 0.17 1
rs11743810 1.000 0.040 5 138466715 intron variant C/T snv 0.50 0.48 1
rs12517396 1.000 0.040 5 44359424 intron variant C/A snv 4.1E-02 1
rs12603825 1.000 0.040 17 1770111 intron variant G/A;T snv 1
rs12965607 1.000 0.040 18 49864655 intron variant T/G snv 1.0E-01 1
rs13380104 1.000 0.040 15 79086479 intron variant C/T snv 0.43 1
rs17428076 1.000 0.040 2 171987022 intron variant C/G snv 0.18 1
rs1793639
NTM
1.000 0.040 11 132061637 intron variant G/A snv 0.39 1
rs200329677 1.000 0.040 22 45973898 intron variant C/T snv 1.4E-05 1
rs201140091 1.000 0.040 10 48200198 intron variant A/-;AAAAA;AAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA delins 1
rs2155413 1.000 0.040 11 84923746 intron variant C/A snv 0.55 1
rs2207136 1.000 0.040 6 50842007 intron variant T/C snv 0.34 1
rs2342406 1.000 0.040 2 44925609 intron variant T/C snv 0.19 1
rs2839471 1.000 0.040 21 42134346 intron variant C/T snv 0.39 1
rs2853559
VDR
1.000 0.040 12 47889022 intron variant A/G snv 0.68 1
rs2908972 1.000 0.040 17 11503942 intron variant T/A snv 0.39 1