Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587778556
NFE2L2
2 177231705 missense variant G/A snv 3.2E-05 4.9E-05 2
rs755135182
NFE2L2
2 177231657 missense variant G/A snv 4.0E-06 2
rs1005752506
AMPH
7 38461398 missense variant G/A snv 7.0E-06 1
rs1235134025
CAST
5 96740769 missense variant C/T snv 4.0E-06 1
rs1300858963
OGA
10 101799033 missense variant G/A snv 4.0E-06 1
rs1348073540
ARHGAP22 ; MAPK8
10 48431259 missense variant C/G;T snv 4.0E-06 1
rs1411928276
DCT
13 94479251 missense variant C/T snv 1
rs1424794503
MFGE8
15 88899478 missense variant G/A snv 8.0E-06 1
rs281860580
HLA-B ; HLA-C
6 31270083 missense variant G/A;T snv 1
rs376388064
VEGFA
6 43782006 missense variant C/T snv 2.8E-05 3.5E-05 1
rs752410089
CAST
5 96741548 missense variant C/G;T snv 4.0E-06 7.0E-06 1
rs760073870
CAPN2
1 223752954 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs768194029
NFATC2
20 51523286 missense variant G/A;C snv 4.0E-06 1
rs769483065
HSP90AA1
14 102085426 missense variant G/A;T snv 8.0E-06 1
rs775645890
UPK3B
7 76515192 missense variant C/T snv 1
rs776045205
CAST
5 96747369 missense variant C/A;T snv 6.4E-05; 2.4E-04 1
rs779612015
UPK3B
7 76515186 missense variant C/T snv 4.7E-06 1
rs780325052
CAST
5 96746417 missense variant C/T snv 2.0E-05 3.5E-05 1
rs893595382
DLG4
17 7196908 missense variant G/A snv 4.0E-06 7.0E-06 1
rs398122403
SYNJ1
0.807 0.080 21 32695106 missense variant C/T snv 1.2E-05 11
rs763872192
CD36
0.882 0.080 7 80672000 missense variant C/T snv 2.8E-05 4
rs201792381
APP
1.000 0.080 21 25997384 missense variant G/A;C snv 1.6E-05 2
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7