Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2
rs13294439 1.000 0.040 9 23358877 intron variant A/C snv 0.32 2
rs34808376 0.925 0.040 7 155456016 intron variant -/GC delins 2
rs6150410 0.925 0.040 7 155454910 intron variant CGCATCCCC/-;CGCATCCCCCGCATCCCC delins 0.28 2
rs194085 1.000 0.040 5 9591303 intergenic variant A/G snv 0.15 1
rs73598374
ADA
0.790 0.280 20 44651586 missense variant C/A;G;T snv 7.1E-06; 6.2E-02 8
rs379863
ADA
1.000 0.040 20 44632053 intron variant C/T snv 0.73 1
rs6551665
ADGRL3
0.882 0.040 4 61873823 intron variant G/A snv 0.59 4
rs2236624
ADORA2A-AS1 ; SPECC1L-ADORA2A ; ADORA2A
0.925 0.200 22 24440056 intron variant T/C snv 0.80 2
rs765619798
ADRA1A
0.925 0.040 8 26864720 missense variant C/A;T snv 2
rs370956755
ADRA2B
0.925 0.040 2 96115984 missense variant C/A;T snv 4.0E-06; 1.6E-05 2
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs766483232
APBA2
1.000 0.040 15 29114003 missense variant A/C;G snv 4.0E-06; 3.6E-04 1
rs465899
APC
0.882 0.160 5 112841474 synonymous variant G/A snv 0.65 0.60 3
rs1804197
APC
1.000 0.040 5 112844212 3 prime UTR variant C/A snv 7.2E-02 2
rs4446909
ASMT
0.925 0.040 Y 1614890 upstream gene variant G/A snv 2
rs5989681
ASMT
1.000 0.040 Y 1614999 upstream gene variant G/A;C snv 1
rs35424709
ATP13A4
0.925 0.040 3 193454190 missense variant T/A snv 8.6E-02 7.8E-02 2
rs2278556
ATP2B2
0.925 0.040 3 10360419 intron variant G/A snv 0.34 2
rs35678
ATP2B2
0.925 0.040 3 10338239 missense variant C/T snv 0.49 0.47 2