Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 2
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs1876829
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs2076529
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 2
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 1
rs12440667
LOXL1
1.000 0.040 15 73939098 intron variant C/A;T snv 1
rs1254319
C14orf39
1.000 14 60437039 missense variant G/A snv 0.35 0.36 1
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 1