Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 1
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 1
rs6759952
DIRC3
1.000 0.080 2 217406996 intron variant T/A;C snv 1
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 1
rs1443434
FOXE1
0.851 0.080 9 97855197 3 prime UTR variant G/T snv 0.63 1
rs1443435
FOXE1
1.000 0.080 9 97855301 3 prime UTR variant T/C snv 0.63 1
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 1
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 1
rs2439302
NRG1
0.776 0.200 8 32574851 intron variant G/C snv 0.54 1
rs12348691
PTCSC2
0.925 0.120 9 97846400 intron variant G/A snv 0.63 1
rs7028661
PTCSC2
0.882 0.080 9 97776188 intron variant A/G snv 0.72 1
rs1867277
PTCSC2 ; FOXE1
0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63 1
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1
rs10984103 0.925 0.080 9 97876993 TF binding site variant A/C snv 0.68 2
rs7866436 0.925 0.080 9 97887814 intergenic variant G/A snv 0.70 2
rs907580 0.851 0.080 9 97860315 downstream gene variant T/A;C;G snv 2
rs925487 0.925 0.080 9 97874116 regulatory region variant C/A;T snv 2
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 2
rs2060793
CYP2R1
0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 2
rs10983700
PTCSC2
1.000 0.080 9 97775173 intron variant T/A;C snv 2
rs1588635
PTCSC2
1.000 0.080 9 97775520 intron variant A/C snv 0.72 2
rs7024345
PTCSC2
0.925 0.080 9 97832956 intron variant A/G snv 0.82 2
rs7030280
PTCSC2
1.000 0.080 9 97772985 intron variant C/T snv 0.72 2
rs7848973
PTCSC2
0.925 0.080 9 97826557 intron variant A/G snv 0.67 2