Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1993709
LOC105378797
1.000 0.080 1 72372846 intron variant A/G snv 0.85 3
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 3
rs34668726
KLHL29
1.000 0.040 2 23673031 intron variant C/G snv 0.13 3
rs3764002
LOC105369965 ; WSCD2
1.000 0.080 12 108224853 missense variant C/T snv 0.27 0.20 3
rs3936510
C5orf67
1.000 0.040 5 56565039 intron variant G/A;T snv 3
rs10152595
SMAD3
1.000 0.080 15 67183150 intron variant C/G;T snv 2
rs10260148
LOC105375508
1.000 0.080 7 130746210 intergenic variant C/T snv 0.27 2
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 2
rs1254319
C14orf39
1.000 14 60437039 missense variant G/A snv 0.35 0.36 2
rs1278493
PPP2R3A
1.000 0.080 3 136095167 intron variant G/A;C snv 2
rs1294421
LOC101928004
1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 2
rs1334576
RREB1
1.000 0.040 6 7211585 missense variant G/A snv 0.45 0.40 2
rs146095395
TWIST2
1.000 0.080 2 238861244 intron variant C/T snv 0.12 2
rs2057884
SRPK2
1.000 0.040 7 105289803 intron variant T/C snv 0.59 2
rs2452877 1.000 0.040 5 4027643 regulatory region variant A/G snv 0.60 2
rs2526882
PCNX1
1.000 0.040 14 70907985 synonymous variant G/A;C snv 0.62 2
rs622217 1.000 0.080 6 160345738 upstream gene variant T/A;C snv 2
rs7235891
LOC105372130
1.000 0.040 18 55787543 intron variant T/C snv 0.55 2
rs758801
STAB1
1.000 0.040 3 52502292 intron variant A/C snv 0.86 2
rs809955
MAML3
1.000 0.040 4 139953606 intron variant G/A snv 0.38 2
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 2
rs1020731
RBMS1
1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 1
rs11075985
FTO
1.000 0.080 16 53771295 intron variant C/A snv 0.42 1