Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs8181047
CDKN2B-AS1
0.807 0.120 9 22064466 intron variant A/G snv 0.79 6
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs1192415 0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81 3
rs1647381 1.000 0.040 15 56794001 intron variant C/G snv 0.12 3
rs17752199 0.925 0.040 6 51542050 upstream gene variant A/C;G;T snv 3
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 3
rs6478746 0.925 0.040 9 126605119 intron variant G/A snv 0.72 3
rs9853115 0.925 0.040 3 186413811 intergenic variant T/A;G snv 0.51 3
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 3
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 3
rs2151280
CDKN2B-AS1
0.701 0.360 9 22034720 non coding transcript exon variant G/A snv 0.46 3
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs944801
CDKN2B-AS1
0.882 0.120 9 22051671 intron variant G/A;C snv 3
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 3
rs9913911
GAS7
0.925 0.040 17 10127866 intron variant A/G snv 0.32 3
rs2745572
LOC102723944
0.925 0.040 6 1548134 intergenic variant A/G snv 0.31 3
rs2472493
LOC105376196
0.851 0.040 9 104933567 downstream gene variant G/A snv 0.61 3
rs11024102
PLEKHA7
0.851 0.040 11 16987058 intron variant T/C snv 0.20 3
rs1015213 0.851 0.040 8 51974981 intron variant C/T snv 0.14 2
rs1254276 1.000 0.040 14 60380283 intergenic variant C/G;T snv 2