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
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
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
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs72928038
BACH2
0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs10936599
MYNN
0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 15
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
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 7
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7