Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs11247287
PCSK6
15 101365328 intron variant T/C snv 0.34 1
rs17199964
BANK1
4 101786634 intron variant G/A;C snv 5
rs1398607 1.000 0.080 3 102036894 TF binding site variant C/A;T snv 2
rs17779355 10 102168617 downstream gene variant G/A snv 4.1E-02 1
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs10778215
C12orf42
12 103143488 intron variant T/A;G snv 2
rs200911786 4 103253686 upstream gene variant C/A;T snv 1
rs12893623
PPP1R13B
14 103824476 intron variant A/G snv 0.29 1
rs1092913
ROPN1L
0.925 0.080 5 10467590 intron variant G/A snv 0.19 1
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 5
rs2740488
ABCA1
0.827 0.120 9 104899461 intron variant A/C snv 0.29 9
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 6
rs1800978
ABCA1
1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 6
rs1799777
ABCA1
9 104903754 5 prime UTR variant -/C delins 0.10 1
rs4455790
RP1L1
8 10634174 intron variant C/G snv 0.74 2
rs10861661
RIC8B
12 106780868 intron variant A/C snv 0.23 1
rs78011072
BTBD11
12 107647896 intron variant A/G snv 6.7E-03 1
rs9657541
PINX1
8 10785654 intron variant C/G;T snv 0.17 1
rs6995541
PINX1
8 10813750 intron variant A/G;T snv 1
rs11776767
MIR1322 ; PINX1
8 10826419 intron variant G/C;T snv 1
rs752273 2 108314649 upstream gene variant T/A snv 0.23 2
rs149793040
ACACB
12 109223867 missense variant A/G snv 7.6E-04 8.4E-04 1