Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs620861
PCAT1 ; CASC8 ; POU5F1B ; CASC21
0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 1
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs6931262
RREB1
6 7217284 non coding transcript exon variant C/T snv 0.10 1
rs9491696
RSPO3
6 127131494 intron variant C/G snv 0.45 1
rs7745274
RSPO3 ; LOC112267972
6 127188012 intron variant G/A snv 0.56 1
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 1
rs6701231
TBX15
1 118953038 intron variant C/A;G snv 1
rs984222
TBX15
1 118961220 intron variant C/A;G snv 1
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs1406948
UQCC1
20 35317816 intron variant G/A snv 0.44 1
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 1
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 1
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs12714415 2 651430 intergenic variant T/C snv 0.19 2
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs634869 6 139510620 intron variant T/A;C snv 2
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 2
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 2