Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs7849782
GRIN3A
0.925 0.160 9 101664982 intron variant C/A;G;T snv 3
rs9485729 1.000 0.120 6 102688156 intergenic variant C/T snv 0.27 1
rs549908
IL18
0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs3762491
SLC35F5
1.000 0.120 2 113731675 intron variant G/A snv 1.9E-02 4.3E-02 1
rs11793049
ZNF618
0.925 0.120 9 114011589 intron variant A/G;T snv 2
rs17136627
LOC101927078 ; KCNN2
0.925 0.120 5 114463289 intron variant C/T snv 7.5E-02 2
rs2244234 1.000 0.120 8 11478958 upstream gene variant T/G snv 0.83 1
rs2409780 1.000 0.120 8 11480078 intron variant T/C snv 0.25 1
rs1564267 0.925 0.160 8 11480378 non coding transcript exon variant T/A;C;G snv 2
rs2618444 0.925 0.160 8 11480861 intron variant A/C;T snv 2
rs62489069 1.000 0.120 8 11480874 intron variant A/G snv 0.29 1
rs35393613 1.000 0.120 8 11480957 intron variant C/A;G;T snv 1
rs1531577 1.000 0.120 8 11481052 non coding transcript exon variant C/T snv 0.71 1
rs13256690 1.000 0.120 8 11481059 non coding transcript exon variant G/A;C;T snv 1
rs2061831 0.925 0.160 8 11482373 upstream gene variant T/C snv 0.25 2
rs2736332 0.925 0.160 8 11482456 upstream gene variant G/C;T snv 2
rs7812879 0.807 0.320 8 11482672 upstream gene variant T/A;C snv 6
rs2254891 1.000 0.120 8 11483620 upstream gene variant G/A;C snv 1
rs2736335 1.000 0.120 8 11483978 upstream gene variant A/C;G;T snv 1
rs2736336 0.925 0.160 8 11484361 upstream gene variant G/A;C;T snv 2
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 5
rs2736338 1.000 0.120 8 11484374 upstream gene variant A/C;T snv 1