Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6784615
NISCH
1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 2
rs3851294
DSTYK
1 205161285 missense variant A/G;T snv 0.93 2
rs1552286
NUDT18
8 22107291 3 prime UTR variant C/T snv 0.90 0.88 1
rs9988
GGA3 ; NUP85
17 75234761 synonymous variant C/T snv 0.86 0.85 1
rs598346
SYTL2
11 85725656 synonymous variant A/G;T snv 0.86; 4.0E-06 1
rs2151131
TEX10
9 100346659 intron variant C/G snv 0.84 0.85 1
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs1250259
FN1 ; LOC105373868
1.000 0.040 2 215435759 missense variant T/A snv 0.76 0.79 5
rs2271613
DNAH17
17 78427016 synonymous variant G/A snv 0.74 0.65 1
rs747249
ZBTB44-DT
11 130401752 intron variant A/G;T snv 0.71 1
rs1805741
PHC1
12 8921663 synonymous variant C/T snv 0.69 0.62 1
rs1139653
DNAJA3
16 4434395 missense variant A/T snv 0.68 0.69 1
rs757110
ABCC8
0.851 0.080 11 17396930 missense variant C/A;T snv 0.64; 8.0E-06 6
rs2526882
PCNX1
1.000 0.040 14 70907985 synonymous variant G/A;C snv 0.62 2
rs1053593
HMGXB4
22 35264882 missense variant G/C;T snv 8.0E-06; 0.58 2
rs719802
TTC12
11 113363957 intron variant T/C;G snv 0.56; 8.3E-06 2
rs11718898
CAND2
3 12807323 missense variant T/C snv 0.56 0.71 1
rs2276824
PBRM1
3 52603470 intron variant C/G snv 0.54 0.61 3
rs11085744
QTRT1
19 10709291 missense variant C/G;T snv 0.53 2
rs3736485
DMXL2
15 51456413 non coding transcript exon variant A/G snv 0.50 0.50 2
rs1787013
CEP192
18 13072980 intron variant T/A;C snv 0.45 1
rs1334576
RREB1
1.000 0.040 6 7211585 missense variant G/A snv 0.45 0.40 2
rs668871
SLC22A3
6 160348779 synonymous variant C/G;T snv 0.45 0.50 2
rs2076529
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2
rs7102
LITAF
16 11548386 3 prime UTR variant T/C snv 0.39 0.37 1