Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2789588 6 72433995 intergenic variant A/C snv 0.26 1
rs10462023
PER2
2 238275940 intron variant G/A snv 0.31 0.27 1
rs4583255
TAOK2
16 29977620 intron variant A/G snv 0.36 1
rs1655285
TSNAX-DISC1 ; TSNAX
1 231563728 intron variant G/C snv 9.5E-02 1
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs17069122 6 108002555 downstream gene variant G/A snv 1.9E-02 2
rs17075286 3 43189231 intergenic variant C/G snv 5.9E-02 2
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs2155907 11 98223945 intergenic variant C/T snv 0.38 2
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs2841307 6 100308811 intergenic variant C/T snv 0.20 2
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs6589386 1.000 0.040 11 113573031 intergenic variant C/T snv 0.36 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2
rs6913660 1.000 0.040 6 27123646 upstream gene variant C/A snv 0.14 2
rs6932590 1.000 0.040 6 27281152 downstream gene variant T/C snv 0.26 2
rs7727102 5 4720472 intron variant G/C snv 0.32 2
rs7912580 1.000 0.040 10 62156213 regulatory region variant G/A snv 7.6E-02 2
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs6024905
BPI
20 38329435 intron variant G/A snv 0.47 2
rs245914
CHN2 ; CPVL
1.000 0.040 7 29178543 intron variant G/A;T snv 2
rs6444931
CLDN11
3 170445686 intron variant G/A snv 0.85 2