Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10180496 1.000 0.040 2 12828774 intron variant A/G snv 0.15 1
rs10811723 1.000 0.040 9 22542286 intergenic variant A/G snv 0.55 1
rs1108343 1.000 0.040 16 51177684 non coding transcript exon variant T/C snv 0.52 1
rs11166135 1.000 0.040 1 98883280 intergenic variant A/G snv 0.10 1
rs12602978 1.000 0.040 17 27240054 intron variant C/T snv 9.3E-02 1
rs1352724 1.000 0.040 5 107747786 intergenic variant C/A snv 0.15 1
rs1429138 1.000 0.040 4 147361190 regulatory region variant T/A;C snv 1
rs1884302 0.851 0.120 20 7125642 intron variant T/C snv 0.41 1
rs263771 1.000 0.040 2 185056965 intergenic variant C/A;T snv 1
rs28822480 1.000 0.040 18 60257590 intergenic variant G/A snv 0.25 1
rs34559440 1.000 0.040 17 70402971 intergenic variant T/C snv 0.28 1
rs4816017 1.000 0.040 20 7673726 intergenic variant G/A snv 0.24 1
rs5922945 1.000 0.040 X 84268007 intergenic variant C/T snv 0.25 1
rs72694438 1.000 0.040 1 103822256 intergenic variant G/A snv 0.18 1
rs7918807 1.000 0.040 10 9978231 intergenic variant T/C snv 0.53 1
rs9308447 1.000 0.040 1 9372331 downstream gene variant C/T snv 0.27 1
rs9831002 1.000 0.040 3 18811205 intron variant T/G snv 0.59 1
rs5831974
AAK1
1.000 0.040 2 69477204 intron variant -/A delins 0.60 1
rs1383934
ADAMTS3
1.000 0.040 4 72551807 intron variant G/A snv 0.68 1
rs80270335
ALK
1.000 0.040 2 29393789 intron variant C/T snv 6.5E-02 1
rs1594318
ALLC
1.000 0.040 2 3686354 intron variant C/G;T snv 1
rs10242311
ATXN7L1
1.000 0.040 7 105633273 intron variant A/C snv 6.2E-02 1
rs1122171
C5orf66
1.000 0.040 5 135174297 intron variant C/T snv 0.56 1
rs72748935
CA12
1.000 0.040 15 63347217 intron variant T/C snv 0.39 1
rs3737665
CA6
0.925 0.080 1 8970905 missense variant C/G;T snv 4.0E-06; 0.26 1