Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs78534766
ADCY7
0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs3807307
IRF5
0.827 0.120 7 128939148 intron variant T/C snv 0.41 6
rs35074907
KEAP1
0.807 0.160 19 10489742 synonymous variant G/A snv 1.9E-02 1.5E-02 6
rs114558062 0.851 0.040 3 187923342 intergenic variant T/C snv 6.6E-03 5
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs970987 0.851 0.040 9 21585266 regulatory region variant C/A snv 0.55 5
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5