Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4813376
RIN2
20 19870811 intron variant T/G snv 0.86 2
rs6444931
CLDN11
3 170445686 intron variant G/A snv 0.85 2
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 2
rs993804
RARB
3 25070680 intron variant C/T snv 0.75 2
rs7248363
PGPEP1
19 18357076 intron variant T/C snv 0.74 2
rs2312147
VRK2
1.000 0.040 2 57995793 intron variant T/C snv 0.70 2
rs6046396
RIN2
20 19871859 non coding transcript exon variant G/A snv 0.68 2
rs4996815 13 105999312 intron variant G/T snv 0.61 2
rs2018368 11 10718819 intergenic variant C/G snv 0.59 2
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 2
rs1009080 1 29958713 intergenic variant G/A snv 0.54 2
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 1
rs6024905
BPI
20 38329435 intron variant G/A snv 0.47 2
rs10949808 7 156255955 intergenic variant T/G snv 0.45 2
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 3
rs11789407
LOC105376249
9 118597268 intergenic variant C/A snv 0.44 2
rs4309482
LOC105372125
0.925 0.040 18 55083238 intergenic variant A/G snv 0.39 2
rs12966547
LOC105372125
0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 2
rs2155907 11 98223945 intergenic variant C/T snv 0.38 2
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 6
rs6589386 1.000 0.040 11 113573031 intergenic variant C/T snv 0.36 2
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 2
rs4583255
TAOK2
16 29977620 intron variant A/G snv 0.36 1
rs11164835
DIPK1A
1 92913536 intron variant G/A snv 0.35 2
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 3