Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 15
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 12
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 12
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 12
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 10
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 10
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 9
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 9
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 8
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 8
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7