Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs7597593
ZNF804A
0.827 0.160 2 184668853 intron variant T/C snv 0.53 6
rs183042538
ZHX3
0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs10144845
YLPM1
1.000 0.040 14 74771067 intron variant C/T snv 0.62 2
rs199505
WNT3 ; LRRC37A2
0.925 0.120 17 46782044 intron variant A/G snv 0.84 4
rs734312
WFS1
0.790 0.240 4 6301627 missense variant G/A snv 0.55 0.42 10
rs55814513
WFS1
1.000 0.040 4 6301470 missense variant G/A;T snv 4.0E-03 2
rs1801206
WFS1
4 6300980 stop gained C/G;T snv 0.63 1
rs1801213
WFS1
4 6291969 synonymous variant C/G snv 0.72 0.68 1
rs17711053
VWC2L
1.000 0.040 2 214574984 intron variant A/G snv 0.11 2
rs2717043
VRK2
1.000 0.040 2 57951884 intron variant C/T snv 0.70 2
rs885861
VIPR2 ; LINC00689
7 159028856 3 prime UTR variant G/A snv 0.43 1
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs3819325
UBA7 ; MIR5193
1.000 0.040 3 49806290 non coding transcript exon variant T/C;G snv 0.38; 7.9E-04 2
rs11214589
TTC12
1.000 0.040 11 113374326 intron variant G/A snv 0.36 2
rs2298489
TTC12
1.000 0.040 11 113364697 splice region variant A/G snv 0.61 2
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs10950393
TMEM106B
1.000 0.040 7 12223920 intron variant T/C snv 0.50 2
rs4630333
TIMELESS
0.882 0.040 12 56443632 intron variant C/T snv 0.33 4
rs80278479
TFAP2D
0.925 0.040 6 50758466 intron variant C/G snv 3.0E-03 3
rs896686
TCF4-AS1 ; TCF4
1.000 0.040 18 55455800 intron variant T/G snv 0.12 2
rs12963463
TCF4
1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs599550
TCF4
1.000 0.040 18 55585157 intron variant G/A;T snv 3