Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs2274432
TSEN15
1 184051811 missense variant G/A snv 0.33 0.28 4
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 4
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs1106529
TBX15
1 118988874 intron variant G/A snv 0.77 3
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 3
rs12731372 1 118310352 regulatory region variant C/T snv 0.19 3
rs17396340
KIF1B
1 10226118 intron variant G/A;C snv 3
rs714515
DNM3 ; PIGC
1 172383850 intron variant G/A snv 0.46 3
rs10912872 1 171387110 intergenic variant G/T snv 0.38 2
rs12048049
TGFB2
1 218423955 intron variant C/G snv 0.37 2
rs12127195 1 221136075 upstream gene variant G/A snv 0.33 2
rs12143789
TBX15
1 118954531 intron variant G/C snv 0.13 2
rs3897379 1 219586391 regulatory region variant A/G snv 0.79 2
rs4537555
HHAT
1 210504207 intron variant A/G snv 8.2E-02 2
rs72666268
FGGY
1 59655756 intron variant A/G snv 8.1E-02 2
rs765751
LYPLAL1-AS1 ; LOC107985272
1 219495884 intergenic variant T/C snv 0.59 2
rs2815752
LOC105378797
0.925 0.200 1 72346757 intron variant G/A snv 0.62 1
rs3101457
C1orf100
1 244369912 intron variant G/A snv 0.80 1