Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 3
rs12258967
CACNB2
10 18439030 intron variant C/G;T snv 3
rs12627514 1.000 0.040 21 43339560 intergenic variant C/A;G;T snv 3
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 3
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs17725246
NPC1L1
7 44542387 upstream gene variant T/A;C snv 3
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 3
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 3
rs687914
PRKCE ; LOC102724965
2 45651621 5 prime UTR variant G/A;T snv 3
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 3
rs2236295
ADO
10 62805132 missense variant G/C;T snv 0.32 2
rs2493296
PRDM16
1 3410468 intron variant C/G;T snv 2
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 2
rs4818833
HSF2BP
21 43569666 intron variant A/G snv 2
rs56388530
NPNT
4 105989801 intron variant C/A;T snv 2
rs6686889 1 24703979 upstream gene variant C/A;G;T snv 2
rs6731302
LINC01122
1.000 0.080 2 58606358 intron variant A/G;T snv 2
rs67330701
MYEOV
11 69312240 intron variant C/A;T snv 2
rs6770911
MECOM
3 169577976 intron variant A/C;G;T snv 2
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 2
rs943346
SORBS1
10 95494548 intron variant C/G;T snv 2
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 2