Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5747327
BCL2L13
22 17686446 intron variant T/A;C;G snv 1
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs1968252
LOC105372263
19 7782850 upstream gene variant G/A;T snv 5
rs11428934
CA11 ; SEC1P
19 48640988 intron variant -/G ins 4
rs575404063 19 18405498 intergenic variant AAA/-;A;AA;AAAA;AAAAA delins 4
rs73036517
MARK4 ; EXOC3L2
19 45241584 intron variant A/G snv 0.20 4
rs930232
CNN2
19 1036019 intron variant G/A;C snv 0.44 1
rs147694761
NPC1
18 23571654 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 5
rs16978075
LINC01478 ; LINC01601
18 44533186 intron variant T/C snv 8.5E-02 5
rs398032702
C18orf25
18 46245574 intron variant AA/-;A;AAA;AAAA;AAAAAAA;AAAAAAAAAAAAA delins 4
rs1025687
MAPK4
18 50621423 intron variant T/C snv 0.61 3
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs146890554
CSF3
17 40017384 3 prime UTR variant C/T snv 9.6E-03 5
rs34762051 17 40007650 downstream gene variant AA/-;A;AAA delins 0.31 5
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03 5
rs675600
LINC02210 ; LINC02210-CRHR1
17 45618793 upstream gene variant A/T snv 0.14 4
rs12936529
PIGL
17 16265470 intron variant C/T snv 0.42 3
rs377079849
NAA38 ; CHD3
17 7884458 intron variant ATATATATATAT/-;AT;ATAT;ATATAT;ATATATAT;ATATATATAT;ATATATATATATAT;ATATATATATATATAT;ATATATATATATATATAT;ATATATATATATATATATAT;ATATATATATATATATATATAT;ATATATATATATATATATATATAT;ATATATATATATATATATATATATAT;ATATATATATATATATATATATATATAT;ATATATATATATATATATATATATATATAT delins 0.46 3
rs5820258
ARHGAP23
17 38437623 intron variant CC/-;C;CCC;CCCC;CCCCC delins 3
rs7405635 17 40204299 regulatory region variant T/C snv 0.34 3
rs8068017 17 1417822 downstream gene variant T/A;C snv 3