Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 5
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 5
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 5
rs174541
FADS2
1.000 0.080 11 61798436 intron variant T/C snv 0.29 4
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 4
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 4
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 4
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 3
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 3
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 3
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 3
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 3
rs6420094
SLC34A1
1.000 0.080 5 177390635 intron variant A/G snv 0.29 3