Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs150844304
TP53BP1
15 43434427 intron variant A/C;G snv 4
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 4
rs2943646 2 226234818 intergenic variant A/C;G snv 3
rs5471
TXNL4B ; HP
0.882 0.160 16 72054562 5 prime UTR variant A/C;G snv 7.9E-03 3
rs10489615
GALNT2
1 230169242 intron variant A/C;G snv 2
rs11765979
LOC105375508
7 130761118 intergenic variant A/C;G snv 2
rs2322549
INPP4B
4 142395874 intron variant A/C;G snv 2
rs4285028
SLC15A2
1.000 0.080 3 121941817 3 prime UTR variant A/C;G snv 2
rs7254723
CLPTM1
1.000 0.080 19 44952664 intron variant A/C;G snv 2
rs7847628
PHF19
9 120868947 intron variant A/C;G snv 2
rs2058804
KCTD10
12 109471206 missense variant A/C;G snv 0.50 1
rs255054 16 67983453 upstream gene variant A/C;G snv 1
rs6822892
PDGFC
4 156813523 intron variant A/C;G snv 1
rs2980875 8 125469505 intron variant A/C;G;T snv 4
rs9863753
STAB1
3 52495883 intron variant A/C;G;T snv 2
rs10937241
ETV5
3 186104985 non coding transcript exon variant A/C;G;T snv 1
rs2652834 15 63104668 intron variant A/C;G;T snv 1
rs180349 0.925 0.200 11 116741111 intergenic variant A/C;T snv 3
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 3
rs10955992 8 120860224 intergenic variant A/C;T snv 2
rs970548
MARCHF8
10 45517829 intron variant A/C;T snv 2
rs10743940
CD163
12 7498542 intron variant A/C;T snv 1
rs1945391 11 122649583 regulatory region variant A/C;T snv 1
rs486394
LINC02702
1.000 0.040 11 116655605 intron variant A/C;T snv 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30