Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1261114
TCF4
1.000 0.040 18 55271138 intron variant G/A snv 0.46 2
rs1289543302
ABCB1
0.763 0.440 7 87536472 missense variant C/T snv 12
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs12938775
PAFAH1B1
1.000 0.040 17 2671527 intron variant G/A;T snv 2
rs12963463
TCF4
1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs12967855
CELF4
1.000 0.040 18 37558282 intron variant A/G snv 0.52 2
rs13060816
BBX
1.000 0.040 3 107561639 intron variant T/A;C snv 2
rs13122395
EMCN
1.000 0.040 4 100829496 intron variant G/A snv 0.34 2
rs1322281
PTPRD
1.000 0.040 9 10582445 intron variant T/C snv 0.76 2
rs13296664 1.000 0.040 9 117684418 downstream gene variant C/T snv 0.22 2
rs13381817
TCF4
1.000 0.040 18 55230988 non coding transcript exon variant C/T snv 6.2E-02 2
rs13413953
ARHGAP15
1.000 0.040 2 143479467 intron variant T/G snv 0.25 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs1360380 1.000 0.040 9 23378490 intron variant G/A;T snv 2
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1375194
LOC105374455
1.000 0.040 2 33601810 intron variant T/C snv 0.42 2
rs1382119307
CDSN ; PSORS1C1
6 31116450 missense variant C/G snv 7.0E-06 1
rs138472420
BICRA
1.000 0.040 19 47657765 intron variant G/A snv 3.3E-03 3
rs1409851868
EPHA3
0.882 0.080 3 89399325 missense variant A/G snv 6
rs141746753 1.000 0.040 8 56934154 intergenic variant C/T snv 3.1E-03 3
rs1422192
LINC00461
1.000 0.040 5 88663205 intron variant G/A;T snv 2
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs1427027 1.000 0.040 18 37666359 intron variant C/G;T snv 2