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
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
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
rs2516399 0.925 0.120 6 31513522 upstream gene variant A/G snv 0.11 3
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 3
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 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
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 3
rs174549
FADS2 ; FADS1
0.851 0.240 11 61803910 5 prime UTR variant G/A snv 0.26 3
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18 3
rs9373124
HBS1L
6 135102071 intron variant T/C snv 0.33 3
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs10934582 3 122294507 downstream gene variant G/A snv 0.28 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 2
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 2
rs4328821 3 128597592 intergenic variant A/G snv 0.13 2