Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs979090956
ABCB1
0.827 0.200 7 87553822 missense variant G/C snv 5
rs9479
PML
0.851 0.120 15 74036235 3 prime UTR variant A/G snv 0.50 6
rs9400241
FOXO3
0.882 0.120 6 108682786 3 prime UTR variant C/A;G snv 4
rs927698341
RUNX1T1
0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs924607
LOC105374608 ; LOC100996325
0.851 0.120 5 609978 intron variant C/T snv 0.32 7
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs885822
PRF1
0.882 0.120 10 70598821 missense variant G/A;C snv 0.64 3
rs880028
FIGNL1 ; DDC
0.882 0.120 7 50502438 intron variant A/G snv 0.21 3
rs80338880
TFR2
0.732 0.360 7 100633100 stop gained G/C snv 7.0E-06 12
rs797045145
HFE ; LOC108783645
0.807 0.240 6 26091479 stop gained G/A snv 6
rs786205155
ETV6
0.882 0.120 12 11884481 missense variant T/C snv 4
rs7853758
LOC105376116 ; SLC28A3
0.851 0.120 9 84286011 synonymous variant G/A snv 0.15 0.19 5
rs7809758
DDC ; FIGNL1
0.882 0.120 7 50505635 intron variant A/G snv 0.36 3
rs780246573
HFE ; LOC108783645
0.732 0.360 6 26092860 stop gained C/G;T snv 4.0E-06; 8.0E-06 12
rs7789635 0.882 0.120 7 50405912 downstream gene variant T/C snv 0.40 4
rs777926364
CYP3A5 ; ZSCAN25
0.882 0.120 7 99664017 missense variant C/T snv 4.2E-06 3
rs772470710
NSD2
0.882 0.120 4 1961074 missense variant G/A snv 4.0E-06 3
rs770998368
ERCC5 ; BIVM-ERCC5
0.827 0.240 13 102861511 missense variant C/G;T snv 4.0E-06 5
rs76996680
LEF1
0.882 0.120 4 108163665 missense variant G/A snv 1.0E-03 3.4E-04 3
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs768315648
NR3C1
0.882 0.120 5 143399830 missense variant T/C snv 1.2E-05 3
rs766916111
ITPA
0.882 0.120 20 3223452 missense variant T/C snv 4.0E-06 7.0E-06 3
rs759602460
CNDP2
0.882 0.120 18 74518552 missense variant C/G snv 1.6E-05; 4.0E-06 3
rs757891309
MTR
0.882 0.120 1 236850389 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs757874631
CBL
0.882 0.120 11 119278211 missense variant T/A;C snv 4