Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11285463
LIN28B
6 104944130 intron variant TT/-;T;TTT delins 1
rs113772882
LOC105375123
7 1602560 intergenic variant G/A;T snv 1
rs114285994
LOC105371116
16 19924441 intergenic variant G/A;C snv 1
rs11534296 9 80667487 intergenic variant G/A;C snv 1
rs11578152 1 102111465 intergenic variant A/G;T snv 1
rs11715566
LOC107986022
3 117843589 intron variant C/A;T snv 1
rs11767400
CADPS2
7 122520688 intron variant C/A;T snv 1
rs11893331
CCDC85A
2 56350271 intron variant A/C;G;T snv 1
rs12472911
LRP1B
2 141470940 intron variant C/A;T snv 1
rs12603280 17 6131434 intergenic variant G/A;C snv 1
rs12879819 14 77958440 intergenic variant C/A;G;T snv 1
rs12926791
WWP2
16 69815643 intron variant C/A;G;T snv 1
rs13053505 22 38849613 intergenic variant G/A;C;T snv 1
rs1398217
SKOR2
18 47225867 intron variant G/C;T snv 1
rs1400974
LOC105373831
2 198773966 upstream gene variant G/A;C snv 1
rs1456522 2 198904459 intron variant A/G;T snv 1
rs17817628
LOC107985002 ; STXBP4
17 55097366 intron variant A/C;G snv 1
rs17817995 17 55335233 intergenic variant G/A;C snv 1
rs17854357
CFL1 ; SNX32
11 65834089 splice region variant G/C;T snv 0.12; 5.8E-05 1
rs1860826
MAD1L1
7 2072871 intron variant G/A;T snv 1
rs1888072 9 89591072 intron variant T/C;G snv 1
rs1915146
CTBP2
10 125157645 intron variant A/C;G;T snv 1
rs1973284
AKT3
1 243693379 intron variant A/G;T snv 1
rs201205097 2 613044 intergenic variant -/AC delins 1
rs2063730
GAB2
11 78337478 intron variant A/C;G snv 1