Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 3
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
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
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
rs1876829
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2
rs2287019
QPCTL
1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs2076529
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2