Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1408579
ERLIN1
1.000 0.040 10 100152437 intron variant C/T snv 0.32 3
rs12784396
CWF19L1
0.925 0.040 10 100267650 5 prime UTR variant C/A;T snv 2
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs2373459
SPIC
12 101480178 intron variant C/T snv 0.68 1
rs1037116 15 101528701 upstream gene variant C/T snv 0.20 2
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs13135092
SLC39A8
4 102276925 intron variant A/G snv 5.1E-02 4
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs2923084
CAND1.11 ; AMPD3
11 10367235 intron variant A/G snv 0.29 1
rs4743758
NIPSNAP3A
9 104753533 intron variant C/T snv 0.37 1
rs2494748
AKT1
14 104792555 intron variant C/T snv 0.51 0.48 2
rs2740480
ABCA1
9 104800276 intron variant G/A snv 0.60 1
rs45490496 14 104806341 downstream gene variant A/T snv 0.45 2
rs4983559 14 104810872 downstream gene variant G/A;C snv 1
rs3824477
ABCA1
9 104826047 intron variant G/A snv 5.8E-02 1
rs4149310
ABCA1
9 104826853 intron variant A/T snv 0.34 3
rs7024300
ABCA1
9 104827286 intron variant C/T snv 5.8E-02 1
rs4149307
ABCA1
9 104827463 intron variant C/T snv 0.34 1
rs2853579
ABCA1
9 104828991 synonymous variant G/T snv 0.20 0.23 3
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 1
rs2472386
ABCA1
1.000 0.040 9 104839260 intron variant G/A snv 0.47 1
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs11789603
ABCA1
9 104884738 intron variant C/T snv 0.11 2
rs4149268
ABCA1
1.000 0.040 9 104884939 intron variant C/T snv 0.46 1