Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12443252 15 90521458 intergenic variant C/A;G;T snv 1
rs12623454 2 120568721 intergenic variant G/C;T snv 1
rs12896104 14 73839311 downstream gene variant A/G;T snv 1
rs12942207
LOC102724532
17 47890928 downstream gene variant C/A;T snv 1
rs1323438
PAPPA
9 116353252 intron variant T/A;C snv 1
rs144843919
SUZ12P1
17 30710321 intron variant G/A;T snv 1
rs1547669 6 33807864 upstream gene variant A/G;T snv 1
rs1819436
LINC00446 ; OBI1-AS1
13 78006148 intron variant T/A;C snv 1
rs186606513
CNNM3
2 96816264 5 prime UTR variant G/A;C;T snv 2.2E-02; 4.6E-05; 1.4E-04 1
rs1937436
PDE4B
1 65975646 intron variant G/A;T snv 1
rs1981627 5 134502489 upstream gene variant A/C;G;T snv 1
rs2045457
GPR139
16 20034793 intron variant G/A;T snv 1
rs220193 21 42161198 regulatory region variant A/G;T snv 1
rs2307024
ABCC9
12 21852069 intron variant T/A;G snv 4.0E-06; 0.38 1
rs2324499
LINC00598
13 40087864 intron variant G/A;C snv 1
rs2779165
UHRF1 ; ARRDC5
19 4915435 intron variant G/C;T snv 1
rs2807319 1 22227683 intergenic variant A/G;T snv 1
rs28457693
PTCH1
9 95455066 intron variant A/C;G;T snv 1
rs2934844
PDE10A
6 165728968 intron variant A/C;G;T snv 1
rs3806315
PTPN14
1 214551325 5 prime UTR variant G/A;C snv 1
rs3965156
LRIG1
3 66434532 intron variant A/C;T snv 1
rs4350272
LOC105376456
10 24767189 intergenic variant A/G;T snv 1
rs4511593
TNFSF12-TNFSF13 ; TNFSF12
17 7552219 intron variant C/A;G;T snv 1
rs4679760
KCNAB1
3 156137629 intron variant C/A;G;T snv 1
rs4908404 1 28365223 upstream gene variant T/A;C snv 1