Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35 17
rs1926447
CPB2 ; CPB2-AS1
0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs3870369 1.000 0.080 6 153261855 intron variant T/G snv 0.65 2
rs139064549
COL11A1
1.000 0.080 1 102888579 missense variant G/C snv 8.6E-03 8.8E-03 1
rs9309464
EXOC6B
1.000 0.080 2 72306834 intron variant A/G snv 0.38 1
rs11621270
IFT43
1.000 0.080 14 76064583 intron variant A/G snv 0.16 1
rs2850542
ME2
1.000 0.080 18 50877190 upstream gene variant G/T snv 0.54 1
rs210967
ROS1
1.000 0.080 6 117303386 intron variant C/G snv 0.62 1
rs10870273
STK32C
1.000 0.080 10 132232632 intron variant A/G snv 0.72 1
rs13057743
TBC1D22A
1.000 0.080 22 47110264 intron variant G/A snv 0.25 1