Source: GWASCAT ×
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 18
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
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
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T 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
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 8
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 7
rs174601
FADS2
0.925 0.080 11 61855668 non coding transcript exon variant C/A;T snv 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 7
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 5
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 5
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 5
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 5