Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10231759 7 150815084 regulatory region variant T/C snv 0.41 1
rs1029534
JAZF1
7 28149464 intron variant T/C;G snv 1
rs1043515
PIP4K2B
17 38765943 3 prime UTR variant A/G snv 0.46 1
rs1047014
ID4
6 19841262 3 prime UTR variant T/C snv 0.23 1
rs10472828 5 32888712 non coding transcript exon variant C/T snv 0.40 1
rs10475992
FBXW11
5 171908289 intron variant C/T snv 0.42 1
rs10492321
SOCS2
12 93586312 downstream gene variant T/A snv 0.20 1
rs10513137
ZBTB38
3 141424588 intron variant G/A;C snv 1
rs1051431
MPHOSPH9
12 123161256 synonymous variant G/A snv 0.74 0.63 1
rs1052483 2 219069626 non coding transcript exon variant G/T snv 0.13 1
rs1074683
PXMP4
20 33716847 intron variant C/G snv 0.24 1
rs10748128 12 69433878 intergenic variant G/T snv 0.42 1
rs10770705
SLCO1C1
12 20704533 intron variant A/C snv 0.70 1
rs10799445 1 227724182 upstream gene variant A/C snv 0.27 1
rs10804515
ZBTB20
3 114983210 intron variant A/G snv 0.60 1
rs10838708
PSMC3
11 47419962 intron variant G/A snv 0.39 1
rs10838798
PTPRJ
11 48069751 intron variant T/G snv 0.56 1
rs10838801
PTPRJ
11 48076728 intron variant G/A snv 0.56 1
rs10843164
CCDC91
12 28416781 intron variant T/C snv 0.22 1
rs10859563
LOC101928731 ; CRADD
12 93726563 intron variant C/G snv 0.40 1
rs10863936
DTL
1 212064456 intron variant G/A snv 0.59 1
rs10874746
DIPK1A
1 92858414 intron variant T/A;C snv 1
rs10906982
ADAMTSL3
15 83899406 intron variant T/A snv 0.63 1
rs10935120
CEP63
3 134514250 intron variant A/G snv 0.63 1
rs10948222
SUPT3H
6 45276678 intron variant T/C snv 0.40 1