Disease: Blood Protein Measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 16
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs492602
LOC105447645 ; FUT2
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 7
rs679574
FUT2 ; LOC105447645
0.827 0.120 19 48702851 intron variant C/G snv 0.45 7
rs2227551
PLAU
0.827 0.120 10 73909432 intron variant G/C;T snv 6