Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2004038
ADAMTS7
1.000 0.040 15 78779064 intron variant G/A snv 0.33 2
rs2608029
PVT1
1.000 0.040 8 128157880 intron variant C/G snv 0.37 2
rs78442819
TEKT5
1.000 0.040 16 10647125 intron variant G/C snv 0.13 2
rs1056562
MPZL2
1.000 0.040 11 118254910 3 prime UTR variant T/C snv 0.57 1
rs10758203 1.000 0.040 9 33421422 intergenic variant G/A;C snv 1
rs114807680
EPHB1
1.000 0.040 3 135085649 intron variant G/A snv 9.8E-03 1
rs114928225 1.000 0.040 2 118692164 intergenic variant T/A snv 1.0E-02 1
rs116080888 1.000 0.040 6 32618459 intergenic variant C/A snv 1
rs11632038
GALK2
1.000 0.040 15 49314101 intron variant A/G snv 0.15 1
rs116506680 1.000 0.040 6 29813272 upstream gene variant T/A;C;G snv 1
rs117151283
ERICH6B
1.000 0.040 13 45539328 intron variant C/G;T snv 1
rs117634027
LOC101929727 ; RNLS
1.000 0.040 10 88340394 intron variant G/T snv 2.6E-03 1
rs11855650 1.000 0.040 15 70139434 intergenic variant G/T snv 0.39 1
rs148944993
LINC01891
1.000 0.040 2 234452501 intron variant G/A snv 2.0E-03 1
rs17038564
ACTR2
1.000 0.040 2 65268924 3 prime UTR variant A/G snv 5.3E-02 1
rs17078110 1.000 0.040 6 148185476 intergenic variant T/C snv 1.0E-02 1
rs17400427
FAM227B ; FGF7
1.000 0.040 15 49448874 intron variant T/C snv 0.20 1
rs184697115 1.000 0.040 5 16005668 intergenic variant A/G snv 6.3E-03 1
rs190996050 1.000 0.040 5 1048492 downstream gene variant T/C snv 5.7E-03 1
rs191524990
C1D
1.000 0.040 2 68069083 intron variant A/T snv 7.6E-03 1
rs2006209 1.000 0.040 19 41589873 downstream gene variant C/T snv 0.16 1
rs2179920 1.000 0.040 6 33091097 downstream gene variant C/T snv 0.27 1
rs2316515
IRF4
1.000 0.040 6 410848 3 prime UTR variant A/G snv 0.52 1
rs2320614
NAF1
1.000 0.040 4 163148970 intron variant T/C snv 0.38 1
rs2495239
FOXP4-AS1
1.000 0.040 6 41522750 intron variant A/G snv 0.84 1