Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs7149317
TBPL2 ; LOC107984664
14 55435824 intron variant G/A snv 0.70 0.72 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs8019270
TBPL2
1.000 0.080 14 55440454 missense variant C/A;G;T snv 4.0E-06; 0.63; 4.0E-06 2
rs1201378
WDHD1 ; SOCS4
14 55026690 intron variant T/A;C snv 0.57 1
rs3733402
KLKB1
1.000 0.040 4 186236880 missense variant G/A;C snv 0.54 5
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs4652
LGALS3
0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs3742569
FBXO34
14 55351988 missense variant T/C snv 0.40 0.43 1
rs1045002
FBXO34
14 55351799 missense variant T/A;G snv 0.38; 4.0E-05 1
rs10144418
FBXO34
14 55350990 synonymous variant T/C snv 0.37 0.36 1
rs15870
DLGAP5
14 55152593 missense variant A/G;T snv 0.36 1
rs4644
LGALS3
0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs8003279
ATG14
14 55397412 synonymous variant A/G snv 0.28 0.27 1
rs8176740
ABO
9 133256085 missense variant A/T snv 0.25 0.25 2
rs841
GCH1
0.827 0.200 14 54843774 splice region variant G/A snv 0.22 0.22 8
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 9
rs2274271
DLGAP5
14 55188974 missense variant C/T snv 0.17 0.30 1
rs10144326
DLGAP5
14 55177190 synonymous variant A/G snv 0.16 0.29 1
rs7078003
HOGA1
10 97599655 non coding transcript exon variant C/T snv 0.14 0.14 3
rs41272321
ACAD11 ; NPHP3-ACAD11
3 132619502 missense variant T/C;G snv 8.6E-06; 0.11 2
rs17128136
SOCS4
14 55043392 synonymous variant G/A;T snv 7.3E-02 1
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37