Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000005
LINC00945
21 33060745 intron variant G/C snv 0.51 1
rs10045577
WDR36
5 111090753 intron variant C/A;G;T snv 1
rs1004870
HIVEP3
1 41905116 intron variant C/T snv 0.57 1
rs10062687
ANKRD33B
5 10624754 missense variant T/G snv 0.18 0.20 1
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs10083558
CRTC3-AS1 ; LINC01585
15 90659273 intron variant C/A snv 0.30 1
rs10118552 9 90004338 intron variant A/G snv 0.59 1
rs10135205
LOC105378183 ; LOC105370686
14 103316504 regulatory region variant A/G snv 0.54 1
rs10138752
RAD51B
14 68713254 intron variant C/T snv 8.8E-02 5
rs1013910 1 116868761 intergenic variant G/A snv 0.91 1
rs10147992
STXBP6
14 25034593 intron variant A/G;T snv 2
rs10165200
LINC00299
2 8299499 intron variant G/A snv 0.36 2
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs10174238
STAT4
0.724 0.200 2 191108308 intron variant G/A snv 0.70 12
rs10195713 2 157664393 intergenic variant C/T snv 0.89 1
rs10206089 2 61476184 intron variant G/A snv 4
rs10241173 7 124813204 intergenic variant A/C;G snv 1
rs1025687
MAPK4
18 50621423 intron variant T/C snv 0.61 3
rs10265538 7 20502242 intergenic variant T/C snv 0.20 2
rs10283564
INSL6 ; JAK2
9 5075628 intron variant C/G snv 0.23 2
rs1032726
CD200R1
3 112967228 intron variant T/C snv 0.46 2
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs1036332
LINC01221
1 199043349 intron variant A/C snv 0.70 2
rs10409243
S1PR2 ; DNMT1
19 10222312 3 prime UTR variant C/A;G;T snv 6
rs10410864 19 39711776 downstream gene variant T/C snv 0.68 2