Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8150
AANAT ; RHBDF2
0.807 0.160 17 76470935 3 prime UTR variant G/A;C snv 6
rs144733372
PLEKHM1
0.882 0.120 17 45486856 intron variant T/G snv 4
rs4238989
AANAT
0.851 0.120 17 76467306 intron variant C/G snv 0.45 4
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs5569
SLC6A2
0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs2242446
SLC6A2
0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs7189979
SNX29
0.925 0.040 16 12536330 intron variant A/C;G;T snv 3
rs55945116
SEC11A
0.882 0.040 15 84676882 intron variant G/C snv 0.26 4
rs1432441
MAP2K1
0.882 0.040 15 66426943 intron variant G/A snv 0.27 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs1549854
MAP2K1
0.882 0.040 15 66404397 intron variant A/C;G snv 0.44 3
rs3825882
NTRK3
0.925 0.040 15 88126151 intron variant G/C;T snv 2
rs4887379
NTRK3
0.925 0.040 15 88184105 intron variant C/G snv 0.24 2
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs77945277
BAZ1A
0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs2273816
KPNA3
0.851 0.080 13 49719920 intron variant G/A;C snv 4
rs1352618632
STARD13
0.925 0.040 13 33112802 missense variant T/C snv 4.0E-06 2
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 27