Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4738296
KCNB2
1.000 0.040 8 72945304 upstream gene variant A/C snv 7.9E-02 1
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 2
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs2395157
TSBP1-AS1
0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs485774
TSBP1-AS1 ; TSBP1
0.925 0.120 6 32323177 intron variant A/G snv 0.42 0.33 3
rs9268528 0.851 0.280 6 32415331 regulatory region variant A/G snv 0.34 3
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs3115553
TSBP1-AS1
0.851 0.200 6 32278050 intron variant C/T snv 0.25 4
rs10760706
STX17
1.000 0.040 9 99961410 intron variant C/T snv 0.69 1
rs3099624 1.000 0.040 1 11436937 intergenic variant C/T snv 0.34 1
rs7228576
LINC01254 ; LOC105371988
1.000 0.040 18 10408495 intron variant C/T snv 0.19 1
rs12348691
PTCSC2
0.925 0.120 9 97846400 intron variant G/A snv 0.63 1
rs9864529
LPP
1.000 0.040 3 188387268 intron variant G/A snv 0.52 1
rs2666138 1.000 0.040 2 36104014 intergenic variant G/A;T snv 1
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs7682241 1.000 0.040 4 122602720 regulatory region variant G/T snv 0.30 1
rs1024161 0.925 0.160 2 203857029 intergenic variant T/A;C snv 2
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 2
rs3130320
TSBP1-AS1
0.851 0.160 6 32255481 intron variant T/C snv 0.68 4
rs405875 0.925 0.120 6 32247411 intergenic variant T/C snv 0.42 2
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 2
rs11224294 0.925 0.080 11 100578431 regulatory region variant T/C snv 9.9E-02 1