Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62569723
LOC105376219
9 111174639 intron variant A/G;T snv 2
rs200243293
LOC105376219
9 111183336 intron variant G/-;GG delins 2
rs17207368
LOC105376219
9 111191714 intron variant G/A snv 1.9E-02 2
rs540639423
SH2B3
12 111407152 intron variant C/T snv 4.6E-03 2
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs2273788
PTGR1
9 111586337 intron variant C/T snv 0.25 2
rs13271228
TRPS1
8 115585182 intron variant T/A;G snv 2
rs73204034 12 116401216 regulatory region variant C/T snv 6.5E-02 2
rs11580646
TENT5C
1 117619797 intron variant C/G snv 0.14 2
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs11992162 8 11979005 upstream gene variant G/A;C;T snv 2
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs7650082 3 12226280 intergenic variant T/G snv 0.47 2
rs144110170 11 122649353 regulatory region variant C/- delins 0.13 2
rs55793580 9 124247116 regulatory region variant C/T snv 0.16 2
rs10987830 9 128016459 intergenic variant G/A snv 6.8E-03 2
rs34834119
ETS1
11 128463122 intron variant AT/- del 0.26 2
rs117758012
HOOK2 ; MAST1
1.000 0.080 19 12846836 intron variant C/T snv 4.1E-02 3
rs9880192 1.000 0.040 3 128578726 upstream gene variant G/A;C snv 0.31 4
rs6772849 3 128587575 intergenic variant T/A;C snv 0.34 2
rs2734037 3 128590041 intergenic variant C/T snv 0.34 2
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs2712381
RPN1
3 128619757 downstream gene variant A/C snv 0.61 2
rs55683935
RPN1
3 128630533 intron variant T/C;G snv 2
rs10956483
CCDC26
8 129559864 intron variant G/A;C snv 2