Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 7
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 5
rs2954031 8 125479491 intron variant G/T snv 0.42 4
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 4
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 3
rs4794822 17 40000459 downstream gene variant C/G;T snv 3
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 3
rs6936204 0.925 0.160 6 32249315 intergenic variant T/C snv 0.70 2
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 2
rs1334577
RREB1
0.925 0.120 6 7211518 intron variant G/A snv 0.23 2
rs1917445 11 103718366 intron variant C/T snv 0.44 1
rs218265 4 54542832 intergenic variant T/C snv 0.21 1
rs272594 8 80557885 upstream gene variant A/C snv 0.22 1
rs546829 4 74090655 upstream gene variant A/T snv 0.63 1
rs8078723 1.000 0.080 17 40010626 upstream gene variant T/C snv 0.36 1
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 1
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51 1
rs6775745
CPNE4
3 132095056 intron variant G/A;T snv 1
rs2837828
DSCAM
21 40803034 intron variant A/G snv 0.44 1
rs61897795
FADS2
11 61850697 intron variant A/G snv 9.5E-02 1
rs174555
FADS2 ; FADS1
11 61812288 intron variant T/C snv 0.26 1