Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3774959
NFKB1
0.925 0.080 4 102589957 intron variant G/A snv 0.34 1
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 2
rs4574118 1.000 0.080 2 106331987 intergenic variant C/G snv 0.84 1
rs367615 1.000 0.080 5 109613236 intergenic variant C/G;T snv 1
rs11213809
C11orf53
1.000 0.080 11 111265020 intron variant A/G snv 0.74 1
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 2
rs10749971
LOC105369491
1.000 0.080 11 111318433 upstream gene variant A/G snv 0.27 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 1
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55 2
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 4
rs551510
TBX3
1.000 0.080 12 114676231 intron variant C/T snv 0.49 1
rs59336
TBX3
0.776 0.160 12 114678547 intron variant T/A;G snv 0.49 1
rs515746
TBX3 ; LOC105370000
1.000 0.080 12 114681192 intron variant G/A snv 0.49 0.48 1
rs140355816 0.790 0.080 8 116562277 intergenic variant C/G snv 9.8E-03 1
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 2
rs11986063 1.000 0.080 8 116628076 regulatory region variant C/T snv 0.12 1
rs6469656 0.790 0.080 8 116635549 regulatory region variant G/A;C snv 1
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 1
rs1870481 1.000 0.080 4 117741865 intergenic variant C/T snv 0.55 1