Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs165940
LOC107986348 ; PDE4D
0.925 0.040 5 59383658 intron variant A/T snv 0.38 4
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs2514218 0.925 0.040 11 113522272 regulatory region variant C/T snv 0.26 4
rs2619538
DTNBP1
0.882 0.040 6 15664978 upstream gene variant A/T snv 0.54 4
rs3916965 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 4
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs701428
RTN4R
1.000 0.040 22 20241019 downstream gene variant A/G snv 0.56 4
rs7219021
TTLL6
0.925 0.040 17 48763179 intron variant T/G snv 0.26 4
rs7872515
SPTLC1
0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs947267
DAOA-AS1 ; DAOA
0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs10494561
NMNAT2
1.000 0.040 1 183277955 intron variant C/T snv 9.4E-02 3
rs10503929
NRG1
0.925 0.040 8 32756465 missense variant T/C snv 0.13 0.13 3
rs1421292 0.925 0.040 13 105545886 intergenic variant T/A snv 0.39 3
rs17512836
TCF4
0.925 0.040 18 55527730 intron variant T/C snv 2.2E-02 3
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 3
rs2076369
PICK1
0.925 0.040 22 38067645 non coding transcript exon variant T/A;G snv 3
rs2619539
DTNBP1
0.925 0.040 6 15620624 intron variant C/A;G snv 3
rs3788533
PLA2G6
0.925 0.040 22 38127239 non coding transcript exon variant C/G snv 0.47 3
rs4309482
LOC105372125
0.925 0.040 18 55083238 intergenic variant A/G snv 0.39 3
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 3
rs7759855 0.925 0.040 6 28315086 downstream gene variant A/G snv 2.8E-02 3
rs951436 0.925 0.040 1 163063552 regulatory region variant A/C snv 0.42 3