Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2072671
CDA
0.752 0.280 1 20589208 missense variant A/C snv 0.28 0.25 2
rs758801
STAB1
1.000 0.040 3 52502292 intron variant A/C snv 0.86 2
rs7929543 0.925 0.120 11 49329474 intron variant A/C snv 0.12 2
rs10062083
SEMA5A
1.000 0.040 5 9130861 intron variant A/C snv 0.11 1
rs10063061
PHAX
1.000 0.040 5 126608051 intron variant A/C snv 0.26 1
rs10092799 1.000 0.040 8 13757626 intergenic variant A/C snv 8.3E-02 1
rs10094221
C8orf87 ; LOC105375644
1.000 0.040 8 93155425 intron variant A/C snv 0.36 1
rs10166710 1.000 0.040 2 187684313 regulatory region variant A/C snv 4.7E-02 1
rs10242655 1.000 0.040 7 15816551 intergenic variant A/C snv 0.33 1
rs10280963
DPP6
1.000 0.040 7 154189483 intron variant A/C snv 0.41 1
rs1034375
WTAPP1
1.000 0.040 11 102824741 intron variant A/C snv 9.9E-02 1
rs10494629 1.000 0.040 1 190028800 intergenic variant A/C snv 3.4E-02 1
rs10501658
RAB38
1.000 0.040 11 88055724 intron variant A/C snv 6.2E-02 1
rs10510418
PPARG
1.000 0.040 3 12347064 intron variant A/C snv 0.25 1
rs10510482
TBC1D5
1.000 0.040 3 17897237 intron variant A/C snv 6.3E-02 1
rs10512856
CPNE4
1.000 0.040 3 132159854 intron variant A/C snv 0.10 1
rs10513388
TTLL11
1.000 0.040 9 122054719 intron variant A/C snv 9.0E-02 1
rs10517030
PPARGC1A
0.925 0.120 4 23961283 intergenic variant A/C snv 6.9E-02 1
rs10517378
LINC02505
1.000 0.040 4 36530747 intron variant A/C snv 0.10 1
rs10768074 1.000 0.040 11 34422964 regulatory region variant A/C snv 0.14 1
rs10787875 1.000 0.040 10 118878029 intron variant A/C snv 0.36 1
rs10818618
TTLL11
1.000 0.040 9 122036961 intron variant A/C snv 0.21 1
rs10833472
NELL1
1.000 0.040 11 21170986 intron variant A/C snv 0.46 1
rs10839272 1.000 0.040 11 49377421 intron variant A/C snv 0.12 1
rs10862344
PPFIA2
1.000 0.040 12 81697021 intron variant A/C snv 0.98 1