Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80358261
NPC2
0.925 0.160 14 74486404 missense variant C/T snv 1.7E-05 1.4E-05 3
rs121434444
KIF5A
0.882 0.160 12 57569648 missense variant C/T snv 2.8E-05 7.0E-06 4
rs28939711
CUTC ; COX15
0.851 0.120 10 99724057 missense variant G/A snv 3.2E-05 3.5E-05 5
rs74315322
HAX1
1.000 0.040 1 154275165 stop gained C/T snv 3.6E-05 3
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs121908345
MLC1
0.827 0.240 22 50080391 missense variant G/A snv 1.3E-04 6.3E-05 6
rs141138948
EXOSC3
0.807 0.120 9 37783993 missense variant T/C;G snv 4.1E-04 9
rs1800014
PRNP
0.776 0.200 20 4699875 missense variant G/A snv 8.0E-03 2.2E-03 11
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs1064039
CST3
0.827 0.200 20 23637790 missense variant C/G;T snv 0.20 6
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs13963
CLEC3B ; EXOSC7
3 45035631 missense variant G/A snv 0.49 0.43 1
rs1051169
S100B
0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65 5