Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 3
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs3760627
CLPTM1
1.000 0.080 19 44953923 non coding transcript exon variant T/C snv 0.80 0.51 2
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs1048699
PPP1R37 ; MARK4
1.000 0.080 19 45147128 3 prime UTR variant C/T snv 9.0E-02 2
rs689
INS ; INS-IGF2
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 1
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 3
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2