Disease: Protein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 13
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 6
rs2280401
SNORD35B ; RPS11
19 49496752 intron variant G/A snv 0.12 5
rs3733402
KLKB1
1.000 0.040 4 186236880 missense variant G/A;C snv 0.54 5
rs4985726
TNFRSF13B
0.925 0.120 17 16960324 intron variant C/G snv 0.11 5
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 4
rs4273077
TNFRSF13B
0.925 0.160 17 16945825 intron variant A/G snv 0.13 4