Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs853679
ZSCAN31
0.851 0.160 6 28329086 intron variant C/A snv 0.20 4
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs12476147
ZNF804A
0.851 0.040 2 184936178 missense variant A/T snv 0.66 0.59 4
rs183042538
ZHX3
0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs139459337
ZBTB20
0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs35792458
XKR6
0.925 0.040 8 10964921 intron variant G/C snv 0.53 3
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs11155372
UTRN
0.925 0.040 6 144698602 intron variant G/C;T snv 3
rs9321987
UTRN
0.925 0.040 6 144709148 intron variant C/T snv 0.40 3
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs352759
TUSC3
0.925 0.040 8 15742205 intron variant T/A snv 3
rs4570625
TPH2
0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs4290270
TPH2
0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs7305115
TPH2
0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs120074175
TPH2
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs1800532
TPH1
0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs10514299
TMEM161B-AS1
0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
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
rs2984618
TAL1
0.925 0.040 1 47224766 intron variant G/T snv 0.52 3
rs1352618632
STARD13
0.925 0.040 13 33112802 missense variant T/C snv 4.0E-06 2