Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs10496702
NCKAP5
2 133247997 intron variant G/A snv 0.18 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs11164835
DIPK1A
1 92913536 intron variant G/A snv 0.35 2
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs11789407
LOC105376249
9 118597268 intergenic variant C/A snv 0.44 2
rs12282742
SAA2-SAA4 ; SAA2
11 18244252 intron variant C/G;T snv 2
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 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
rs1992044
LOC105375856 ; LINC01602
8 57928349 intron variant G/A;T snv 2
rs1992045
LOC105375856 ; LINC01602
8 57928365 intron variant C/T snv 0.14 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs2044117
NALCN ; NALCN-AS1
13 101055958 intron variant G/A snv 0.19 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
rs4813376
RIN2
20 19870811 intron variant T/G snv 0.86 2
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs6024905
BPI
20 38329435 intron variant G/A snv 0.47 2
rs6046396
RIN2
20 19871859 non coding transcript exon variant G/A snv 0.68 2
rs6444931
CLDN11
3 170445686 intron variant G/A snv 0.85 2
rs6627057 X 145059799 downstream gene variant T/G snv 0.16 2