Disease: Protein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs2731672
GRK6
5 177415473 intron variant T/C snv 0.66 6
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 4