Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 1
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 1
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs4640244
KCNJ12
17 21380911 intron variant A/G snv 0.33 1
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 1
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs11154370 6 126846446 intron variant A/G;T snv 1
rs757608 17 61419916 regulatory region variant A/G;T snv 1
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 2
rs605203
EHMT2-AS1 ; LOC107986588 ; CYP21A2 ; SLC44A4
1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs6701231
TBX15
1 118953038 intron variant C/A;G snv 1
rs984222
TBX15
1 118961220 intron variant C/A;G snv 1
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 3