Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 9
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 9
rs2266780
FMO3
0.827 0.280 1 171114102 missense variant A/G snv 0.15 0.14 9
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs2266782
FMO3
0.851 0.200 1 171107825 missense variant G/A snv 0.37 0.41 7
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7
rs2274700
CFH
0.776 0.240 1 196713817 synonymous variant G/A;C;T snv 0.44 6
rs2306235
PLEKHO1
0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs12037879
LEPR
0.925 0.080 1 65477024 intron variant G/A;T snv 5
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs9332978
CYP4A11
0.882 0.040 1 46942278 upstream gene variant T/C snv 7.3E-02 5
rs10489177
C1orf112 ; METTL18
0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 4
rs1126742
CYP4A11
0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 4
rs17111503
PCSK9
0.925 0.160 1 55037775 upstream gene variant A/G snv 0.22 4
rs1800247
BGLAP ; PMF1-BGLAP
0.882 0.200 1 156242034 intron variant T/C snv 0.20 4
rs198358
NPPA-AS1 ; CLCN6
0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 4
rs2235543
HSD11B1-AS1 ; HSD11B1
0.925 0.080 1 209687323 intron variant T/A;C snv 4
rs2746071
RGS2
0.882 0.160 1 192808434 intron variant A/G snv 0.35 4
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 4
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs5051
AGT
0.882 0.160 1 230714126 intron variant C/A;G;T snv 4