Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1411832 1.000 0.040 10 106126497 intergenic variant C/T snv 0.10 2
rs536551654 1.000 0.120 17 49511972 missense variant T/C snv 2
rs61748411 0.925 0.120 X 154031356 missense variant T/C snv 3
rs1397094538 0.925 0.120 1 23367044 missense variant A/T snv 4.0E-06 3
rs763868966 1.000 0.080 17 44911429 stop gained C/A;G;T snv 1.2E-05; 4.0E-05 4
rs63751011 0.925 0.120 17 46010418 intron variant C/T snv 4
rs281865071 0.882 0.080 1 154571759 missense variant C/G;T snv 5
rs2732260 0.882 0.200 8 33431749 intron variant G/A snv 8.4E-02 5
rs1977412 0.882 0.160 1 230716523 intron variant T/A;C snv 5
rs8074995 0.925 0.040 17 66796013 intron variant G/A snv 0.13 5
rs7127507 0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs775129479 0.851 0.120 16 1791387 missense variant G/A;C;T snv 1.6E-05; 8.1E-06; 8.1E-06 6
rs781587642 0.851 0.120 2 219250557 missense variant G/A;C snv 2.0E-05 6
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs63750577 0.827 0.120 14 73186881 missense variant C/T snv 8
rs63750852 0.790 0.120 14 73170998 missense variant G/A;T snv 8
rs80356702 0.882 0.120 7 143330868 missense variant G/A snv 4.0E-06 1.4E-05 9
rs1424266770 0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs768823392 0.827 0.120 16 89546657 coding sequence variant GGCGGGAGA/- delins 2.6E-04 4.2E-04 10
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs12273363 0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs1556424691
CYTB ; ND6 ; TRNT
0.851 0.200 MT 15923 non coding transcript exon variant A/G snv 13
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14