Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs148881970 0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs555145190 0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs1556424691
CYTB ; ND6 ; TRNT
0.851 0.200 MT 15923 non coding transcript exon variant A/G snv 13
rs12273363 0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs63751011 0.925 0.120 17 46010418 intron variant C/T snv 4