Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4704397
PDE8B
0.807 0.200 5 77222617 intron variant G/A snv 0.54 13
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 6
rs2622590
XKR4
0.925 0.080 8 55445714 intron variant G/A snv 0.15 4
rs11026407
LOC102723370 ; ANO5
11 22083484 intron variant C/A snv 0.54 2
rs6683419
LOC105376819 ; MICOS10
1 19501286 intron variant G/A snv 0.52 2
rs10818050
PTCSC2
9 97776641 intron variant A/G;T snv 2
rs12126655
VAV3
1 107814198 intron variant A/G snv 0.33 2