Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4821112
UBE2L3
22 21610472 intron variant G/A snv 0.21 4
rs760361706
PPARA
22 46235326 missense variant G/C snv 4.0E-06 4
rs6498142
CLEC16A
16 10987392 intron variant C/G snv 0.77 3
rs926657
TAGAP ; LOC105378083
6 159042420 non coding transcript exon variant C/G;T snv 3
rs1020388 5 56264200 upstream gene variant T/G snv 0.34 2
rs10460003
LINC01882
18 12747013 intron variant C/T snv 0.15 2
rs10752747
MMEL1
1 2593476 intron variant G/T snv 0.41 2
rs10892286
DDX6
11 118771376 intron variant A/C snv 0.17 2
rs10932019 2 203764087 downstream gene variant G/A;C snv 2
rs11043097
LINC02752
11 11114248 intron variant T/C snv 0.15 2
rs1194849
SPRED2
2 65379519 intron variant T/C snv 0.49 2
rs11984075
ELMO1
7 37397251 intron variant A/G snv 0.14 2
rs12138909
MMEL1
1 2607299 intron variant C/T snv 0.11 2
rs1355208 2 30222456 intergenic variant A/G snv 0.65 2
rs1772408
IFI16
1 159035859 intron variant A/G;T snv 2
rs1876518
SPRED2
2 65381775 intron variant C/T snv 0.45 2
rs2155433 11 118742212 intron variant G/A snv 0.24 2
rs2893008
IL21-AS1
4 122631659 intron variant A/G snv 5.1E-02 2
rs4288027
KIAA1109
4 122262050 intron variant A/C;G snv 0.13 2
rs4374642
KIAA1109
4 122179956 intron variant T/C snv 0.13 2
rs4626515 7 140204330 intergenic variant T/C snv 0.22 2
rs636393 6 137686393 intron variant G/T snv 0.66 2
rs6706689
PUS10
2 60943910 intron variant A/G snv 0.48 2
rs7678445
KIAA1109
4 122361617 intron variant G/A;T snv 2
rs9295089
LOC105378083 ; TAGAP
6 159042932 non coding transcript exon variant T/C snv 0.20 2