Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 2
rs9926095
NKD1
1.000 0.040 16 50645404 3 prime UTR variant A/C;T snv 1
rs991804 1.000 0.040 17 34260706 downstream gene variant C/T snv 0.33 1
rs9891119
STAT3
0.882 0.120 17 42355962 intron variant A/C snv 0.36 2
rs9875617
BSN
1.000 0.040 3 49597263 intron variant G/A;C;T snv 1
rs9858542
BSN
0.925 0.040 3 49664550 synonymous variant G/A snv 0.26 0.27 2
rs9827708
BSN
1.000 0.040 3 49612556 intron variant C/G snv 0.29 1
rs9822268
APEH
0.925 0.040 3 49682296 intron variant G/A;T snv 2
rs9812791
BSN
1.000 0.040 3 49644878 intron variant G/A snv 0.28 1
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 1
rs968567
FADS2 ; FADS1
0.851 0.240 11 61828092 intron variant C/T snv 0.11 3
rs9562532
NRAD1
1.000 0.040 13 44025653 non coding transcript exon variant G/A snv 0.61 1
rs9525625
LINC02341
1.000 0.040 13 42443894 intron variant T/C snv 0.45 1
rs9491697
RSPO3
1.000 0.040 6 127134977 intron variant A/G snv 0.41 1
rs941823
LINC00598
0.827 0.120 13 40439840 intron variant T/C snv 0.77 2
rs9358372
CDKAL1
1.000 0.040 6 20812357 intron variant G/A snv 0.64 1
rs9297145
KPNA7
0.827 0.120 7 99161494 intergenic variant C/A snv 0.67 1
rs9292777 0.925 0.120 5 40437846 regulatory region variant C/T snv 0.60 2
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 3
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs9267911 0.925 0.160 6 32237333 intergenic variant T/C snv 0.45 2
rs9264942
LOC112267902 ; HLA-B
0.763 0.400 6 31306603 intron variant T/C snv 0.34 6