Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12325410
LOC101927026
0.851 0.040 16 9581389 intron variant T/G snv 0.16 5
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs1386482
TPH2
0.827 0.080 12 72018792 intron variant T/G snv 0.52 5
rs1386486
TPH2
0.827 0.080 12 72018440 intron variant A/G snv 0.53 5
rs1534891
CSNK1E ; TPTEP2-CSNK1E
0.827 0.200 22 38299094 intron variant T/C snv 0.90 5
rs166508
ITGA9
0.827 0.080 3 37548944 intron variant T/C snv 0.44 5
rs1705236
TSPAN8
0.827 0.200 12 71151778 intron variant T/A snv 7.6E-02 5
rs2021722
TRIM26
0.851 0.040 6 30206354 intron variant C/A;T snv 0.24 5
rs231779
CTLA4
0.827 0.160 2 203869764 intron variant C/T snv 0.41 5
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs2799573
CACNB2
0.851 0.040 10 18312999 intron variant T/C snv 0.20 5
rs28456
FADS1 ; FADS2
0.925 0.120 11 61822009 intron variant A/C;G snv 5
rs3132581
MUCL3 ; HCG21 ; SFTA2
0.851 0.040 6 30945681 intron variant G/A snv 9.3E-02 5
rs324650
LOC349160 ; CHRM2
0.827 0.080 7 137008914 intron variant T/A snv 0.55 5
rs6465084
LOC105375382 ; GRM3
0.851 0.040 7 86774159 intron variant A/G snv 0.26 5
rs6484218
CAND1.11 ; AMPD3
0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs7004633
LOC105375630
0.851 0.040 8 88748082 intron variant A/G snv 0.28 5
rs7914558
CNNM2
0.851 0.040 10 103016151 intron variant G/A snv 0.40 5
rs839523
ERBB4
0.827 0.080 2 211951364 intron variant C/T snv 0.40 5
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9804190
ANK3
0.882 0.040 10 60080073 intron variant C/T snv 0.30 5
rs10405744
ZNF93
0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 4
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs10761482
ANK3
0.851 0.120 10 60325579 intron variant T/C snv 0.70 4