Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12712133 1.000 0.080 2 102249813 downstream gene variant A/G snv 0.57 1
rs1598856
NFKB1
1.000 0.080 4 102524958 intron variant A/G snv 0.61 1
rs230534
NFKB1
0.882 0.120 4 102527884 intron variant T/C snv 0.73 2
rs17033015 1.000 0.080 4 102625147 intergenic variant A/C snv 0.65 1
rs7665090
MANBA
0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 4
rs1054037
MANBA
1.000 0.080 4 102631552 3 prime UTR variant C/A;T snv 1
rs8017161
EXOC3L4
0.925 0.080 14 103096858 intron variant G/A snv 0.38 2
rs2297067
EXOC3L4
1.000 0.080 14 103100448 missense variant C/T snv 0.22 0.20 2
rs526231 1.000 0.080 5 103345680 intergenic variant C/T snv 0.24 1
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 1
rs2041670
CLEC16A
0.851 0.280 16 11080795 intron variant G/A;C snv 1
rs12708715
CLEC16A
1.000 0.080 16 11083967 intron variant C/T snv 0.39 1
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 1
rs12924729
CLEC16A
0.882 0.200 16 11093926 intron variant G/A snv 0.34 2
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 2
rs12935413
CLEC16A
1.000 0.080 16 11116590 intron variant G/A snv 0.34 2
rs4938534
BTG4 ; POU2AF1
0.925 0.080 11 111404408 intron variant G/A snv 0.56 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs4780355
SOCS1 ; RMI2 ; LOC105371082
0.882 0.120 16 11254001 intron variant T/C;G snv 2
rs1646019
LOC105371082 ; RMI2
1.000 0.080 16 11265823 intron variant C/T snv 0.36 1
rs80073729
RMI2 ; LOC105371082
1.000 0.080 16 11279940 intron variant G/A snv 4.1E-03 1