Disease: Fibrinogen, CTCAE
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 5
rs2073643
SLC22A5
1.000 0.080 5 132387596 intron variant T/C snv 0.46 4