Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
rs697852
ITPKB
1 226727033 intron variant G/A snv 0.82 3
rs9889262
ZNF652
17 49320708 intron variant T/A snv 0.28 3
rs1064213
PLCL1
2 198085516 missense variant G/A snv 0.44 0.41 2
rs11684176
PLCL1
2 198090050 intron variant C/T snv 0.38 2
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 2
rs2134814
BACH2
6 90277793 intron variant C/G snv 0.26 2
rs346835
LINC00299
2 8298563 intron variant C/T snv 0.39 2
rs3540
IQGAP1
15 90502176 3 prime UTR variant G/A snv 0.43 2
rs4850808 2 197711418 intron variant T/A;C snv 2
rs6011033
RTEL1-TNFRSF6B ; RTEL1
20 63691346 intron variant A/G;T snv 2
rs6021268
NFATC2
20 51524602 intron variant T/C snv 5.8E-02 2
rs73078636
DCAF1
3 51403873 intron variant G/A snv 9.7E-02 2
rs7562
FOSL2
2 28412873 3 prime UTR variant T/C snv 0.53 2
rs10033073
STX18-AS1 ; LOC101928279
4 4773674 intron variant A/G snv 0.32 1
rs10068717
NDFIP1
5 142115369 intron variant C/T snv 0.67 1
rs10497813
PLCL1
2 198049348 intron variant G/T snv 0.43 1
rs10663129
RASA2
3 141602994 intron variant -/CT delins 0.29 1
rs10760123
PHF19
9 120888256 intron variant T/A;G snv 1
rs10865050
IL18R1 ; IL1RL1
2 102324851 intron variant G/A snv 0.18 1
rs10883723
MFSD13A ; ACTR1A
10 102466075 5 prime UTR variant T/C snv 0.29 1
rs10893845 11 128316987 regulatory region variant T/G snv 0.36 1
rs10975488
IL33
9 6213829 upstream gene variant A/G;T snv 1
rs111914382
TTC6
14 37627796 intron variant -/G delins 0.20 1