Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 6
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs8098380
YES1
18 721563 downstream gene variant A/C snv 0.33 4
rs13405173
PDE1A
2 182449087 intron variant A/C snv 8.8E-03 3
rs7302816 12 89556543 upstream gene variant A/C snv 0.27 2
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 5
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs6418
GML ; CYP11B2
8 142914947 intron variant A/C;G snv 0.42 4
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 13
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs9375463 6 126845743 intron variant A/C;T snv 3
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs35444 12 115114632 intergenic variant A/G snv 0.38 6