Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9999820
NPY2R
0.925 0.080 4 155197173 intron variant A/G snv 0.66 1
rs999944 1.000 0.080 2 64822719 intergenic variant A/G snv 0.83 1
rs999943
ITPR3
1.000 0.080 6 33656956 intron variant A/G snv 0.28 1
rs9999118
SPATA5
1.000 0.040 4 123130312 intron variant A/G snv 1.2E-02 1
rs999885
AP4M1 ; MCM7
0.925 0.120 7 100103553 intron variant G/A snv 0.56 0.46 1
rs9998368
STIM2
1.000 0.040 4 26887432 intron variant C/T snv 0.62 1
rs9997790
MOB1B ; DCK
4 70993963 missense variant G/A;C snv 4.3E-06; 1.5E-02 2
rs9997649 1.000 0.040 4 152066292 regulatory region variant T/C snv 0.51 1
rs999737
RAD51B
0.776 0.200 14 68567965 intron variant C/T snv 0.16 1
rs9996608
NAAA
4 75927078 intron variant C/T snv 0.29 1
rs9996452
CC2D2A
1.000 0.040 4 15559008 intron variant C/G snv 0.41 1
rs9995997 4 72661796 intergenic variant G/A snv 0.36 1
rs9995716
KLHL2P1
4 119343841 intron variant T/C snv 0.36 1
rs999556 0.925 0.080 5 151094113 upstream gene variant A/G snv 0.38 1
rs9995319
BBS7
4 121849522 intron variant G/C snv 0.29 1
rs9995034
LOC102724158
1.000 0.040 4 121985860 intergenic variant T/A;C;G snv 1
rs999494
EMX1
1.000 0.040 2 72930266 intron variant C/T snv 0.20 1
rs9994759 4 31891570 intergenic variant T/C snv 0.23 1
rs9994441
SH3RF1
1.000 0.080 4 169173411 intron variant G/C snv 0.19 1
rs9994216
SLC2A9
4 9982917 intron variant G/T snv 0.65 1
rs9993636
LOC105374552
4 27977139 intron variant C/T snv 0.83 1
rs9993633
MOB1B ; DCK
1.000 4 70997893 intron variant G/A snv 0.11 5
rs9993613 4 72610297 intergenic variant T/G snv 0.42 1
rs9993475 0.925 0.040 4 28007067 intergenic variant C/T snv 2.9E-02 2
rs9993023
SPINK2
4 56822425 upstream gene variant G/A snv 0.11 1