Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1062708
MIR6798 ; RUVBL2
1.000 0.080 19 49010016 missense variant C/A;G;T snv 4.3E-06; 1.7E-05; 0.48 1
rs1063537
ADIPOQ-AS1 ; ADIPOQ
0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 6
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10744777
ALDH2
1.000 0.080 12 111795214 intron variant T/C snv 0.53 1
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs10849373
NINJ2-AS1 ; NINJ2
1.000 0.080 12 631795 intron variant G/A snv 0.27 1
rs10877887
LINC01465 ; MIRLET7I
0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs10900213
ALOX5
1.000 0.080 10 45409266 intron variant G/A;T snv 1
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 32
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 4
rs10947803
KCNK17
1.000 0.080 6 39302834 intron variant C/A snv 2
rs11018628
NOX4
1.000 0.080 11 89473343 intron variant T/C;G snv 2
rs11052413 1.000 0.080 12 33053704 intergenic variant T/G snv 0.58 1
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs11196288 1.000 0.080 10 113297684 regulatory region variant A/G snv 5.5E-02 2
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs11214109 1.000 0.080 11 112173503 intron variant C/G;T snv 1
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16