Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 5
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs138544659
CHRNA3
1.000 0.040 15 78608359 intron variant T/G snv 0.28 5
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 5
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 5
rs55958997
CHRNB4
1.000 0.040 15 78623530 upstream gene variant C/A snv 0.32 5
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4