Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 3
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 2
rs907094
PPP1R1B
1.000 0.040 17 39634118 intron variant G/A snv 0.69 0.60 1
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 1
rs3743075
CHRNA3
1.000 0.040 15 78617110 missense variant T/A;C snv 4.0E-06; 0.66 1
rs6427339
ARHGEF11
1.000 0.040 1 156984475 intron variant C/T snv 0.47 0.50 1
rs4633
COMT ; MIR4761
0.695 0.400 22 19962712 synonymous variant C/T snv 0.46 0.45 2
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 1
rs6356
TH
0.827 0.240 11 2169721 missense variant C/T snv 0.43 0.32 1
rs1042779
ITIH1
0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 2
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 3
rs9331888
CLU ; MIR6843
0.827 0.200 8 27611345 5 prime UTR variant C/G snv 0.35 0.28 1
rs707939
MSH5-SAPCD1 ; MSH5
0.851 0.200 6 31758911 intron variant C/A snv 0.34 0.26 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 2
rs5174
LRP8
0.776 0.240 1 53247055 missense variant C/T snv 0.29 0.28 1
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs12000
NKAPL ; ZKSCAN4
0.925 0.160 6 28259658 missense variant A/G snv 0.28 0.34 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 1
rs1035130
IL18R1
1.000 0.040 2 102384942 synonymous variant C/T snv 0.26 0.24 1
rs204993
PBX2
0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3
rs950169
ADAMTSL3
1.000 0.040 15 84037709 missense variant C/T snv 0.22 0.19 1
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 4