Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10272006
SP4
0.925 0.080 7 21480514 intron variant G/A snv 0.75 2
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 1
rs10883437 1.000 0.040 10 100035604 regulatory region variant T/A;G snv 0.43 2
rs117542855 1.000 0.040 11 1635713 regulatory region variant C/G;T snv 3.1E-02 1
rs11794552
LOC105376299 ; PLPP7
1.000 0.040 9 131344938 intron variant C/T snv 0.15 1
rs11820744
OSBPL5 ; LOC107987158
1.000 0.040 11 3147308 intron variant C/T snv 0.23 2
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 1
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02 3
rs1227756
COL13A1
0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs12373751
ERBB4
1.000 0.040 2 212072166 intron variant T/C snv 0.62 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1263173 0.925 0.080 11 116810292 downstream gene variant G/A snv 0.53 1
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 1
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 2
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 1
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 2
rs139271658
PTPRD
1.000 0.040 9 9797383 intron variant A/G snv 1.9E-02 2
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 2
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 3
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 2
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1