Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1352618632
STARD13
0.925 0.040 13 33112802 missense variant T/C snv 4.0E-06 2
rs195478 0.925 0.040 6 115851928 intergenic variant C/A;G snv 2
rs2551941
METTL21A
0.925 0.040 2 207627419 upstream gene variant A/G;T snv 2
rs319924
EYS ; PHF3
0.925 0.040 6 63777354 intron variant A/G;T snv 2
rs3825882
NTRK3
0.925 0.040 15 88126151 intron variant G/C;T snv 2
rs4685959 0.925 0.040 3 5645577 regulatory region variant C/G;T snv 2
rs4810896 0.925 0.040 20 48918761 upstream gene variant A/C;G snv 2
rs6320
HTR5A-AS1 ; HTR5A
0.925 0.040 7 155070911 synonymous variant T/A;G snv 0.26; 1.2E-05 2
rs772335034
P2RX2
1.000 0.040 12 132618851 missense variant C/A snv 9.6E-06 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs120074175
TPH2
0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs201921722 0.925 0.040 11 123679999 downstream gene variant -/A delins 9.2E-06 3
rs146486358
CUX1
0.882 0.080 7 102205168 missense variant C/T snv 8.6E-04 3.0E-04 3
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs80278479
TFAP2D
0.925 0.040 6 50758466 intron variant C/G snv 3.0E-03 3
rs143405544
ADAMTS6
0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs77945277
BAZ1A
0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3