Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10838532
LARGE2
1.000 0.080 11 45925913 intron variant G/C snv 0.18 1
rs10846744
SCARB1
0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs10889160
CYP2J2
1.000 0.080 1 59896449 intron variant T/C snv 0.23 1
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10898909
P2RY2
0.925 0.120 11 73241451 non coding transcript exon variant G/A snv 0.21 2
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs10965215
CDKN2B-AS1
0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46 4
rs10986769
MAPKAP1
0.925 0.120 9 125460061 intron variant A/G;T snv 2
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs11234027
NADSYN1
0.882 0.080 11 71523061 intron variant G/A snv 0.24 5
rs1129844
CCL11
0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38 10
rs1131498
C1orf112 ; SELL
0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1131692208
MIR6886 ; LDLR
0.925 0.160 19 11113603 missense variant C/T snv 4
rs1135402763
APOB
1.000 0.080 2 21032540 missense variant T/C;G snv 1
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1144507
ZNF202
0.925 0.080 11 123729767 missense variant A/C;G;T snv 0.68 2
rs1151640
OR13G1
1.000 0.080 1 247672648 missense variant T/C snv 0.46 0.36 1