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
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
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
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs17037452
CLCN6
1 11835618 intron variant A/G snv 0.18 3
rs2980755 8 8506173 intergenic variant A/G snv 0.46 3
rs656319 8 9956901 intergenic variant A/G snv 0.49 3
rs7823056 8 8525195 intergenic variant A/G snv 0.55 3
rs1133322
COX5A
15 74920016 3 prime UTR variant A/G snv 0.38 2
rs13178964 5 105011948 intron variant A/G snv 0.17 2
rs133980 22 27626764 intergenic variant A/G snv 0.42 2
rs60605842
SLC4A7
3 27439550 intron variant A/G snv 0.29 2
rs9561252 13 93077032 intergenic variant A/G snv 7.2E-02 2
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs12946454
ACBD4 ; PLCD3
0.925 0.040 17 45130754 intron variant A/T snv 0.21 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs17613287
CACNB2
10 18430748 intron variant A/T snv 0.27 4
rs1952652
LINC02227
5 158384080 intron variant A/T snv 0.28 3
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9