Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 8
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 7
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 6
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 6
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 6
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6