Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 2
rs10760706
STX17
1.000 0.040 9 99961410 intron variant C/T snv 0.69 1
rs1431704
MIR924HG
1.000 0.040 18 39273770 intron variant T/C snv 7.0E-02 1
rs17479692
SLC16A12
1.000 0.040 10 89528702 intron variant T/G snv 9.3E-02 1
rs2666138 1.000 0.040 2 36104014 intergenic variant G/A;T snv 1
rs3099624 1.000 0.040 1 11436937 intergenic variant C/T snv 0.34 1
rs4738296
KCNB2
1.000 0.040 8 72945304 upstream gene variant A/C snv 7.9E-02 1
rs7099812
MALRD1
1.000 0.040 10 19689469 intron variant T/G snv 0.41 1
rs7228576
LINC01254 ; LOC105371988
1.000 0.040 18 10408495 intron variant C/T snv 0.19 1
rs7682241 1.000 0.040 4 122602720 regulatory region variant G/T snv 0.30 1
rs9479482 1.000 0.040 6 150036876 downstream gene variant T/C snv 0.36 1
rs9864529
LPP
1.000 0.040 3 188387268 intron variant G/A snv 0.52 1
rs9982439 1.000 0.040 21 42329090 regulatory region variant T/C snv 3.1E-02 1
rs11224294 0.925 0.080 11 100578431 regulatory region variant T/C snv 9.9E-02 1
rs485774
TSBP1-AS1 ; TSBP1
0.925 0.120 6 32323177 intron variant A/G snv 0.42 0.33 3
rs405875 0.925 0.120 6 32247411 intergenic variant T/C snv 0.42 2
rs12348691
PTCSC2
0.925 0.120 9 97846400 intron variant G/A snv 0.63 1
rs3130320
TSBP1-AS1
0.851 0.160 6 32255481 intron variant T/C snv 0.68 4
rs1024161 0.925 0.160 2 203857029 intergenic variant T/A;C snv 2
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 2
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs3115553
TSBP1-AS1
0.851 0.200 6 32278050 intron variant C/T snv 0.25 4
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs2395157
TSBP1-AS1
0.827 0.240 6 32380368 intron variant A/G snv 0.24 5
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7