Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs757278
CTTNBP2
1.000 0.120 7 117737591 intron variant G/T snv 0.44 1
rs9414780
JMJD1C
1.000 0.120 10 63241673 intron variant A/C snv 0.87 1
rs9414788
JMJD1C
1.000 0.120 10 63296952 intron variant A/C;G;T snv 1
rs9415699
JMJD1C
1.000 0.120 10 63383798 intron variant T/C snv 0.13 1
rs9415705
JMJD1C
1.000 0.120 10 63401790 intron variant T/G snv 0.13 1
rs953387 1.000 0.120 2 136149600 intergenic variant A/C;T snv 1
rs2372536
ATIC
0.827 0.160 2 215325297 missense variant C/G snv 0.33 0.25 5
rs4750316
LINC02649 ; LINC02656
0.882 0.160 10 6351298 non coding transcript exon variant C/G;T snv 5
rs10954213
IRF5
0.752 0.200 7 128949373 3 prime UTR variant G/A snv 0.58 11
rs11466018
MEFV
0.827 0.200 16 3254739 missense variant A/G snv 6.6E-03 2.2E-03 7
rs12917716
CLEC16A
0.851 0.200 16 11095291 intron variant G/C snv 0.51 4
rs17435
MECP2
0.851 0.200 X 154046529 intron variant T/A;C snv 4
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 3
rs2240337
PADI4
0.925 0.200 1 17347727 intron variant C/T snv 9.5E-02 2
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs7731626
ANKRD55
0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12928404
ATXN2L
0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs62324212
IL21-AS1
0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10988542
FNBP1
0.724 0.240 9 129894985 intron variant G/A;C snv 14