Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003878
TSBP1-AS1 ; TSBP1
0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23 3
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 3
rs1012411 1.000 0.120 6 30364778 upstream gene variant T/G snv 0.32 1
rs1015166
TAP2
0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 1
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs10255021
COL1A2
1.000 0.120 7 94402493 intron variant G/A snv 0.13 1
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 2
rs10484566
PSMB9
0.925 0.200 6 32867481 regulatory region variant T/G snv 6.8E-02 2
rs10492166
CLECL1
1.000 0.120 12 9733403 upstream gene variant G/A snv 0.50 1
rs1050152
SLC22A4 ; MIR3936HG
0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1
rs10509540
LOC101929727 ; RNLS
0.925 0.160 10 88263276 upstream gene variant T/C snv 0.25 2
rs10517086
LINC02357
0.882 0.160 4 26083889 intron variant G/A snv 0.27 2
rs1052486
BAG6
0.851 0.200 6 31642909 missense variant A/G snv 0.51 0.44 1
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 2
rs1053924
PPT2-EGFL8 ; LOC100507547 ; PRRT1 ; PPT2
1.000 0.120 6 32152938 non coding transcript exon variant T/C snv 0.71 1
rs1055569
HCG26 ; HCP5
0.882 0.240 6 31472305 non coding transcript exon variant C/T snv 0.41 2
rs1058026
HLA-B
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 5
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 1
rs1065356
MPIG6B ; LY6G6C
1.000 0.120 6 31719231 synonymous variant G/A snv 0.27 0.31 1
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 1
rs10743152
TH
1.000 0.120 11 2174751 upstream gene variant T/C snv 0.63 1
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 4
rs10770141
MIR4686 ; TH
1.000 0.120 11 2172610 upstream gene variant A/C;G snv 1
rs1077393
BAG6
0.882 0.200 6 31642752 non coding transcript exon variant A/G snv 0.44 3
rs10774654 1.000 0.120 12 112525756 intergenic variant A/G snv 0.20 1