Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 4
rs11012476
NEBL
0.925 0.120 10 21003994 intron variant C/T snv 3.5E-02 3
rs3129900
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32338202 intron variant G/T snv 0.83 3
rs2205986
SYT14
0.925 0.160 1 209942767 intron variant G/A snv 0.92 2
rs6139258
RNF24
1.000 0.080 20 3977969 intron variant T/C snv 3.2E-02 2
rs10404821
C19orf81
1.000 0.080 19 50657831 intron variant C/A;T snv 1
rs10937275
ST6GAL1
1.000 0.080 3 186933001 intron variant A/G snv 0.88 1
rs115266745
LINC01266
1.000 0.080 3 779530 intron variant A/C snv 8.3E-03 1
rs116606120 1.000 0.080 5 28665845 intron variant T/A snv 1.0E-02 1
rs117491755
ASTN2
1.000 0.080 9 116881377 intron variant A/C snv 2.6E-02 1
rs143575776
PTPRD
1.000 0.080 9 9593742 intron variant A/T snv 1.2E-02 1
rs1497546
LOC105373999
1.000 0.080 3 98315682 intron variant G/A snv 9.0E-02 1
rs185305928
CAMTA1
1.000 0.080 1 6845651 intron variant G/A snv 9.3E-03 1
rs191153876
CCDC14
1.000 0.080 3 123918335 intron variant A/T snv 1.4E-02 1
rs2025009
RAD51B ; LOC107984679
1.000 0.080 14 68376888 intron variant G/A;C snv 1
rs2240395
TBXAS1
1.000 0.080 7 140018347 intron variant C/G;T snv 0.41 1
rs2523822 1.000 0.080 6 29860883 intron variant A/G snv 0.26 1
rs28521457
LRBA
1.000 0.080 4 150759175 intron variant G/A;C snv 1
rs73122578
ROBO1
1.000 0.080 3 79310483 intron variant A/C snv 0.27 1
rs7828135
TPD52
1.000 0.080 8 80146584 intron variant T/C snv 0.12 1
rs116561224 1.000 0.080 18 66962261 intergenic variant A/G snv 7.4E-02 2
rs72631567 1.000 0.080 2 5092045 intergenic variant A/G snv 4.5E-02 2
rs10812428 1.000 0.080 9 26614849 intergenic variant C/T snv 0.40 1
rs113206698 1.000 0.080 10 92818147 intergenic variant G/A snv 2.6E-02 1
rs114811931 1.000 0.080 5 161257724 intergenic variant T/C snv 1.8E-02 1