Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 23
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 14
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 13
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 12
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 11
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 10
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 9
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 9
rs3810291
ZC3H4
19 47065746 3 prime UTR variant G/A snv 0.50 9
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 8
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8