Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs301819
RERE
0.882 0.120 1 8441726 intron variant A/G;T snv 1
rs4908760
RERE
1.000 0.040 1 8466082 intron variant G/A snv 0.68 1
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs13076312
LPP
1.000 0.040 3 188371466 intron variant C/T snv 0.44 2
rs13091753
LPP
1.000 0.040 3 188396801 intron variant G/C;T snv 2
rs1559810
LPP
1.000 0.040 3 188406566 intron variant C/A snv 0.36 2
rs9851967
LPP
1.000 0.040 3 188369840 intron variant C/T snv 0.35 2
rs17008723
FOXP1
0.925 0.040 3 71523984 intron variant T/G snv 0.15 1
rs59374417 0.925 0.040 3 119569567 intergenic variant A/C;T snv 1
rs16872571
CLNK
0.925 0.080 4 10725229 intergenic variant C/T snv 0.33 1
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 8
rs2395185
HLA-DRB9
0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs3130473 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 6
rs3131296
NOTCH4
0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs3132580
HCG21 ; SFTA2 ; MUCL3
0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 6
rs3134942
NOTCH4
0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 6
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 5
rs13211318 0.925 0.040 6 32134903 upstream gene variant A/C snv 0.11 5