Disease: Ischemic stroke
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs872129 0.925 0.080 1 203200263 intergenic variant A/G snv 0.19 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3751143
P2RX7 ; LOC105370032
0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs544456198
LDLR
0.790 0.120 19 11116930 missense variant G/T snv 8.0E-06 2.8E-05 9
rs752596535
LDLR
0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs147377392
THBD
0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs17057255
EPHX2
0.925 0.080 8 27503724 missense variant C/T snv 1.3E-02 3.4E-02 2