Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10273424
TMEM225B
0.925 0.080 7 99598450 intron variant T/A snv 0.13 1
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 1
rs8032477
IGF1R
0.851 0.200 15 98711325 intron variant C/A;T snv 2
rs17356907
PGAM1P5
0.925 0.080 12 95633983 intron variant A/G snv 0.28 2
rs17021918
PDLIM5
0.776 0.240 4 94641726 intron variant C/T snv 0.30 2
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2
rs941764
CCDC88C
0.925 0.080 14 91374725 intron variant A/G snv 0.46 1
rs8042680
PRC1-AS1 ; PRC1
0.882 0.160 15 90978107 intron variant C/A snv 0.54 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 1
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs2725207
PKD2
0.882 0.200 4 88058377 intron variant C/A snv 0.31 3
rs903263
LOC107985046 ; PRKACB
1.000 0.080 1 84156830 intron variant G/A;T snv 1
rs17530068
LOC105377871
0.882 0.120 6 81483392 intergenic variant T/C snv 0.19 1
rs13329835
CDYL2
0.925 0.080 16 80616908 intron variant A/G snv 0.35 1
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 1
rs704010
ZMIZ1
0.851 0.080 10 79081391 intron variant T/C snv 0.71 1
rs7164529
MORF4L1
0.925 0.080 15 78853456 intron variant G/A snv 0.37 1
rs12906542
ADAMTS7P3
0.925 0.080 15 77977130 intron variant A/C;G;T snv 1
rs7821178 0.925 0.080 8 77181601 intergenic variant C/A;G;T snv 1
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 2
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 1
rs2943559
HNF4G
0.925 0.080 8 75505702 intron variant A/G snv 0.12 1
rs12916
HMGCR ; CERT1
0.807 0.240 5 75360714 3 prime UTR variant T/C;G snv 0.37 3
rs6472903
CASC9
0.925 0.080 8 75318066 intron variant G/T snv 0.86 1
rs1154865 0.882 0.160 12 73596057 intergenic variant C/G snv 0.22 2