Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143046984
LOC105370557 ; PCNX1
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02 9
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05 9
rs377429877
STARD13
0.776 0.080 13 33518027 intron variant -/TAA delins 6.0E-02 10
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 10
rs9924886
CDH3
0.776 0.080 16 68710036 intron variant A/C snv 0.25 10
rs10911251
LAMC1
0.790 0.080 1 183112059 intron variant A/C snv 0.37 9
rs16973225
LOC102724001
0.790 0.080 15 81937658 intron variant A/C snv 7.4E-02 9
rs2184857
LOC105373224
0.790 0.080 1 239918447 upstream gene variant A/C snv 0.45 9
rs6720296
LINC01121
0.790 0.080 2 45181130 intron variant A/C snv 0.52 9
rs73975588
NXN
0.790 0.080 17 913501 intron variant A/C snv 9.9E-02 9
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs4768903
DIP2B
0.790 0.080 12 50651666 intron variant A/C;G;T snv 9
rs2250430
PLEKHG6
0.776 0.080 12 6312008 intron variant A/C;T snv 10
rs4450168
SBF2
0.790 0.080 11 10265208 intron variant A/C;T snv 0.12 9
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs147680653 0.708 0.280 6 29785031 intergenic variant A/G snv 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 17
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 11