Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs10769908
STK33
11 8462542 intron variant C/T snv 0.55 3
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 3
rs11231693
MACROD1 ; FLRT1
11 64095140 intron variant G/A snv 0.11 2
rs1344674
ZBTB38
3 141406344 intron variant A/G snv 0.55 2
rs2745353
RSPO3
6 127131790 intron variant C/T snv 0.55 2
rs987052
LINC02135 ; LINC01081
16 86288853 intron variant T/C snv 0.23 2
rs1013443 5 180774114 intergenic variant A/T snv 1.4E-03 1
rs1014242
PDE1C
7 32232693 intron variant C/T snv 0.54 1
rs1021070
CHRNB4
15 78654521 intron variant C/A;G snv 1
rs1021071
CHRNB4 ; LOC112268142
15 78675837 intron variant G/C snv 0.28 1
rs10226228
PDE1C
7 32276001 intron variant A/G snv 0.38 1
rs10236197
PDE1C
7 32252149 intron variant T/C snv 0.41 1
rs10259431
PDE1C
7 32241785 intron variant C/T snv 0.54 1
rs10264177
PDE1C
7 32331250 intron variant A/G snv 0.40 1
rs1028936
HECTD2-AS1
10 91590040 regulatory region variant A/C snv 0.18 1
rs10951331
PDE1C
7 32314762 intron variant A/G snv 0.22 1
rs10958725 8 42669441 intergenic variant T/G snv 0.63 1
rs10958726 8 42680766 intergenic variant G/T snv 0.66 1
rs11071927 15 66968834 intergenic variant C/A snv 0.85 1
rs11072766
IREB2
15 78479204 intron variant C/G;T snv 1
rs11072774
CHRNB4 ; LOC112268142
15 78660355 intron variant C/T snv 0.20 1
rs11072785
CHRNB4 ; LOC112268142
15 78675887 intron variant C/T snv 0.28 1
rs11072787
CHRNB4 ; LOC112268142
15 78680635 intron variant T/C snv 0.34 1