Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs528704957
CADM1
11 115357179 intron variant -/C delins 2.6E-03 1
rs201385905
ECE1
1 21318845 intron variant -/G delins 8.7E-03 1
rs10680802
FTO
16 53726175 intron variant -/GA delins 1
rs34148541
SV2C
5 75903368 intergenic variant -/GT delins 3.0E-04 1
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 4
rs2030323
BDNF
0.925 0.080 11 27706992 intron variant A/C snv 0.83 3
rs2546057 1.000 0.040 19 33829949 intergenic variant A/C snv 0.41 3
rs2820292
NAV1 ; IPO9-AS1
1 201815159 intron variant A/C snv 0.48 3
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 2
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 2
rs11866219 16 69515846 regulatory region variant A/C snv 0.53 2
rs3736594
MRPL33
2 27772914 intron variant A/C snv 0.62 2
rs75641275
DPYD
1 97861577 intron variant A/C snv 0.10 2
rs762705
LSMEM2 ; SEMA3B
3 50276096 non coding transcript exon variant A/C snv 2
rs10196304
LOC105374786
2 67638833 intron variant A/C snv 0.40 1
rs10261878 7 25910925 intergenic variant A/C snv 0.80 1
rs10840060
STK33
11 8478498 intron variant A/C snv 0.45 1
rs11128058 3 88684137 intergenic variant A/C snv 0.59 1
rs11150911 18 75786573 intergenic variant A/C snv 0.55 1
rs11170468 12 39036246 intergenic variant A/C snv 0.20 1
rs11780222
LOC102724687
8 66293006 intergenic variant A/C snv 0.31 1
rs11915371
SAMMSON
3 70490408 intron variant A/C snv 0.21 1
rs12147136
UNC79
14 93605958 intron variant A/C snv 0.69 1