Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131339
STX17-AS1 ; NR4A3
0.925 0.080 9 99865020 3 prime UTR variant A/G snv 0.45 2
rs1405209
NR4A3 ; STX17-AS1
1.000 0.040 9 99823263 intron variant T/C snv 0.33 1
rs11624408
BCL11B
1.000 0.040 14 99246608 intron variant A/G snv 0.34 1
rs10745843
LOC101928937 ; ANKS1B
0.925 0.040 12 99102252 intron variant G/A snv 0.55 2
rs7560357
MGAT4A
1.000 0.040 2 98631357 intron variant T/G snv 0.18 1
rs12618769
MGAT4A
0.882 0.120 2 98623468 3 prime UTR variant C/T snv 0.18 3
rs11647445
GRIN2A
0.925 0.040 16 9833109 intron variant T/G snv 0.35 2
rs1842329 1.000 0.040 12 98170438 intron variant C/T snv 0.35 1
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs9375225 1.000 0.040 6 98140878 intron variant G/T snv 0.41 1
rs12206087 1.000 0.040 6 98135024 intron variant G/A snv 0.39 2
rs12204181 1.000 0.040 6 98131605 intron variant T/C;G snv 1
rs9401634 1.000 0.040 6 98130635 intron variant T/C snv 0.41 1
rs1872841 1.000 0.040 6 98128812 intron variant C/A snv 0.41 1
rs12202969 1.000 0.040 6 98128347 intron variant G/A snv 0.39 1
rs9388171 1.000 0.040 6 98127850 intron variant C/G snv 0.44 1
rs10457441 1.000 0.040 6 98124244 intron variant T/A;C snv 2
rs1487441 1.000 0.040 6 98106018 intron variant G/A snv 0.39 1
rs1906252 0.925 0.120 6 98102413 intron variant C/A;T snv 3
rs9385269 1.000 0.040 6 98100103 intron variant C/T snv 0.44 1
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs1293651 1.000 0.040 11 98024776 intergenic variant G/A;C;T snv 1
rs35425515
SLIT1
1.000 0.040 10 97119904 intron variant T/C snv 9.7E-02 1
rs6728642
FAM178B
0.925 0.040 2 96941334 intron variant A/G snv 0.19 2
rs6746896 0.851 0.120 2 96745212 intergenic variant A/G snv 0.26 4