Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs4841294
MSRA
8 10247558 intron variant C/A;T snv 2
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs7129220
AMPD3 ; CAND1.11
11 10328991 intron variant G/A snv 0.10 5
rs7832708
MSRA
8 10332530 intron variant C/T snv 0.49 4
rs13178964 5 105011948 intron variant A/G snv 0.17 2
rs10096777
RP1L1
8 10660990 intron variant G/A snv 0.61 2
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs4841465
XKR6
8 10962344 intron variant C/G;T snv 3
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs4460079
ARSJ
4 113940144 intron variant C/T snv 0.58 2
rs7658266
ARSJ
4 113942550 intron variant T/A;C snv 2
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs12705959
FOXP2
7 114358191 intron variant C/T snv 0.39 2
rs13255193
FAM167A
8 11451683 intron variant T/C snv 0.47 2
rs10850411 12 114949991 intergenic variant T/C snv 0.34 1
rs35441 12 115115310 intergenic variant C/T snv 0.40 5