Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 2
rs10180496 1.000 0.040 2 12828774 intron variant A/G snv 0.15 1
rs10242311
ATXN7L1
1.000 0.040 7 105633273 intron variant A/C snv 6.2E-02 1
rs10772314
LOC105369658 ; LINC02446
1.000 0.040 12 10551751 upstream gene variant T/A snv 0.47 1
rs10811723 1.000 0.040 9 22542286 intergenic variant A/G snv 0.55 1
rs10851907
CHRNB4
1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 4
rs10987008
PBX3
1.000 0.040 9 125899321 intron variant T/A snv 0.54 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
rs1122171
C5orf66
1.000 0.040 5 135174297 intron variant C/T snv 0.56 1
rs1126477
LTF
0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 1
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 1
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 1
rs11672900
MAMSTR
1.000 0.040 19 48717066 intron variant A/G;T snv 1
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 3
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 11
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
rs1383934
ADAMTS3
1.000 0.040 4 72551807 intron variant G/A snv 0.68 1
rs140357883
MTMR3
1.000 0.040 22 29896823 intron variant T/-;TT;TTT delins 1
rs1429138 1.000 0.040 4 147361190 regulatory region variant T/A;C snv 1
rs1482698
LINC02224
1.000 0.040 5 44539351 intron variant G/C snv 0.30 1
rs149467613
P2RY2
1.000 0.040 11 73232438 intron variant G/A snv 3.3E-02 2
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs1594318
ALLC
1.000 0.040 2 3686354 intron variant C/G;T snv 1