Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918413
LOC112267935 ; GLRA1
1.000 0.120 5 151851470 missense variant G/T snv 3
rs80358261
NPC2
0.925 0.160 14 74486404 missense variant C/T snv 1.7E-05 1.4E-05 3
rs121913223
DHFR
1.000 0.040 5 80633904 missense variant T/A snv 4.0E-06 2
rs1280914556
KHDRBS1
1 32014269 missense variant A/G snv 2.1E-05 2
rs1467252662
GLRA1 ; LOC112267935
5 151851530 missense variant G/T snv 4.0E-06 2
rs756915170
NUP62 ; IL4I1
19 49909654 missense variant T/C snv 4.0E-06 2
rs13963
CLEC3B ; EXOSC7
3 45035631 missense variant G/A snv 0.49 0.43 1
rs1471980111
DNAH8
6 38737948 missense variant G/A snv 4.1E-06 7.0E-06 1
rs374651285
ALB
4 73406645 missense variant G/A snv 1
rs62643364
PRNP
0.851 0.160 20 4699466 synonymous variant A/G;T snv 4.0E-06; 1.4E-04 7
rs1051169
S100B
0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65 5
rs749191312
RBBP9
1.000 0.080 20 18497075 synonymous variant C/T snv 4.0E-06 2
rs771884087
LOC105372630 ; SLPI
1.000 0.080 20 45253726 synonymous variant T/C snv 2
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23