Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs2075302
FAP
0.882 2 162219636 intron variant T/C snv 0.34 5
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18 5
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs10202630 0.882 2 190398199 intergenic variant T/C snv 0.52 4
rs10444776
LOC112268138
0.882 14 105647030 upstream gene variant G/A;T snv 4
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs10937560
MB21D2
0.882 3 192909627 intron variant G/C snv 0.45 4
rs10986284 0.882 9 124236874 intergenic variant A/T snv 0.27 4
rs11746555
SLC22A5
0.882 5 132391341 intron variant G/A snv 0.28 4
rs11785816
LINC00824
0.882 8 128518940 intron variant C/A;G snv 4
rs1199047
CCDC88B
0.882 11 64350711 intron variant A/C snv 0.38 4
rs12980063
CPT1C
0.882 19 49693735 intron variant A/G snv 0.48 4
rs1320344
C12orf42
0.882 12 103493699 intron variant A/G snv 0.64 4
rs13299616
PSMD5 ; CUTALP
0.882 9 120832525 intron variant T/C snv 0.50 4
rs13380830
RAB5C
0.882 17 42145640 intron variant C/G snv 0.29 4
rs142647938
KCNH7
0.882 2 162516642 intron variant C/A;T snv 4
rs145268310 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 4
rs1530687
ARHGAP31
0.882 3 119395668 intron variant G/A snv 0.46 4
rs1549922 0.882 5 159304540 intergenic variant G/A snv 0.56 4
rs1790588
CD226
0.882 18 69867948 intron variant T/C snv 0.55 4
rs1800601
NTRK1 ; SH2D2A
0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 4
rs191252491
ALDH2
0.882 12 111773070 intron variant A/T snv 7.1E-03 4
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4