Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10770705
SLCO1C1
12 20704533 intron variant A/C snv 0.70 2
rs10799445 1 227724182 upstream gene variant A/C snv 0.27 2
rs13210323
ANKS1A
6 35037307 intron variant A/C snv 0.30 2
rs2289125
NOX4
11 89491285 5 prime UTR variant A/C snv 0.69 0.61 2
rs2755237
LINC00598
13 40535292 intron variant A/C snv 0.17 2
rs3103267
DIS3L2
2 232123872 intron variant A/C snv 0.72 2
rs6473015 8 77266249 intergenic variant A/C snv 0.23 2
rs7153027 14 91960878 intergenic variant A/C snv 0.44 2
rs910316
TMED10
14 75159339 intron variant A/C snv 0.45 2
rs991967
TGFB2-OT1 ; TGFB2
1 218442109 3 prime UTR variant A/C snv 0.37 2
rs9969804
IPPK
9 92666838 intron variant A/C snv 0.68 2
rs10236314
ABCB5
7 20676586 intron variant A/C snv 0.90 1
rs10456943 6 121556819 regulatory region variant A/C snv 0.11 1
rs11198898
GRK5
10 119358980 intron variant A/C snv 0.79 1
rs11521830 9 75675924 intergenic variant A/C snv 5.6E-02 1
rs11542436
STRADA ; LIMD2 ; LOC729683
17 63701329 non coding transcript exon variant A/C snv 0.30 1
rs11638850
RFX7
15 56141657 intron variant A/C snv 0.63 1
rs12003361
LOC107987124
9 120093136 intergenic variant A/C snv 9.8E-02 1
rs12076549
TGFBR3
1 91736142 intron variant A/C snv 0.53 1
rs12309133 12 81843061 intergenic variant A/C snv 0.37 1
rs12347137
PAPPA
9 116360442 intron variant A/C snv 0.16 1
rs12459174
ZNF460
19 57293351 3 prime UTR variant A/C snv 0.23 1
rs12676304
PVT1
8 128151049 intron variant A/C snv 0.24 1
rs12903859 15 70493294 intergenic variant A/C snv 0.84 1
rs12909519
MIR4713HG
15 51049670 intron variant A/C snv 0.60 1