Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554785242
ADAMTS13
0.882 0.160 9 133426240 missense variant G/T snv 8
rs1554791280
ADAMTS13
0.882 0.160 9 133442718 missense variant T/C snv 8
rs1554800065
ANKRD26
1.000 0.120 10 27100445 5 prime UTR variant G/C snv 2
rs1556620697
SH2D1A ; STAG2
0.827 0.360 X 124365758 splice region variant C/G snv 10
rs1559810905
IFIH1
0.827 0.240 2 162273810 missense variant T/A snv 9
rs1569008655
RUNX1
21 34799310 stop gained G/A snv 1
rs1569061762
RUNX1
21 34859476 missense variant C/T snv 1
rs1569061768
RUNX1
1.000 0.120 21 34859477 stop gained G/A snv 2
rs160441 1.000 0.040 8 89644760 intron variant T/C snv 0.55 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs17824620
RPH3A
12 112663189 intron variant C/A snv 0.26 2
rs1800812
PDGFRA
1.000 0.080 4 54228462 intron variant G/C;T snv 2
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs190521996
PMM2
0.790 0.320 16 8811660 missense variant T/C snv 2.9E-04 4.1E-04 12
rs2071346
MYC ; CASC11
0.925 0.160 8 127736777 intron variant G/T snv 7.1E-02 3
rs218916 1.000 0.040 8 89688709 intron variant C/T snv 0.67 2
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2274407
ABCC4
0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs2290280
CCNH ; LOC105379066
5 87412904 5 prime UTR variant C/A;T snv 1
rs2297595
DPYD
0.776 0.320 1 97699535 missense variant T/C snv 8.5E-02 8.1E-02 10
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6