Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79184941
FGFR2
0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs113994095
POLG ; MIR6766
0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs77543610
FGFR2
0.667 0.560 10 121520160 missense variant G/C snv 28
rs113994097
POLG
0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs1800012
COL1A1
0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs140291094
STAC3
0.742 0.320 12 57244322 missense variant C/G snv 9.1E-05 3.8E-04 11
rs121912823
CHAT
0.851 0.280 10 49627681 missense variant T/C snv 4.0E-06 6
rs1555669248
TUBB6
0.807 0.280 18 12325970 missense variant T/C snv 6
rs758026634
MRPL43 ; TWNK
0.827 0.240 10 100989280 missense variant G/A;C snv 2.0E-05 5
rs3918253
MMP9
0.925 0.080 20 46010872 intron variant C/T snv 0.43 0.44 2
rs10911193
LAMC1
1.000 0.040 1 183021513 upstream gene variant C/T snv 0.11 1
rs3918256
MMP9
1.000 0.040 20 46012320 splice region variant G/A snv 0.43 0.44 1