Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs157582
TOMM40
0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 5
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 5
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 5
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 4
rs2206277
TFAP2B
0.925 0.080 6 50830813 intron variant C/T snv 0.19 4
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 4
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 3
rs10838681
NR1H3
1.000 0.040 11 47253513 intron variant G/A snv 0.34 3
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 3
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 3
rs17173608
RARRES2
0.807 0.240 7 150339575 intron variant T/G snv 0.11 3
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 3
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 3
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 3
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 3
rs10484092
FRMD6-AS2 ; FRMD6
1.000 0.040 14 51489516 intron variant A/G snv 4.8E-02 2
rs10849915
CCDC63
0.925 0.080 12 110895818 intron variant T/C snv 0.39 2
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 2
rs12988520
UGT1A6 ; UGT1A9 ; UGT1A8 ; UGT1A10 ; UGT1A7
1.000 0.040 2 233698748 intron variant A/C snv 0.51 2
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 2
rs13226650
MLXIPL
1.000 0.040 7 73602675 intron variant A/G snv 0.19 2
rs1412444
LIPA
0.851 0.120 10 89243170 intron variant C/T snv 0.37 2
rs1558162
POU6F2 ; LOC105375238
1.000 0.040 7 39471024 intron variant C/G;T snv 2
rs16940212
ALDH1A2
1.000 0.040 15 58401821 intron variant G/A;T snv 2
rs1797912
PPARG
1.000 0.040 3 12428740 intron variant A/C snv 0.33 2