Disease: Corpuscular Hemoglobin Concentration Mean
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1165178
SLC17A1
0.925 0.120 6 25827288 intron variant A/G snv 0.65 4
rs1165182
SLC17A3
0.925 0.120 6 25837601 intron variant A/G snv 0.65 4
rs1165205
SLC17A3
0.925 0.120 6 25870314 intron variant T/A;G snv 4
rs1165207
SLC17A3
0.925 0.120 6 25865038 intron variant T/C snv 0.64 4
rs1165209
SLC17A1
0.925 0.120 6 25801091 intron variant G/A snv 0.66 4
rs1183200
SLC17A1
0.925 0.120 6 25818418 intron variant G/C snv 0.66 4
rs1183201
SLC17A1
0.925 0.120 6 25823216 intron variant A/T snv 0.65 4
rs1184803
SLC17A3
0.925 0.120 6 25834430 intron variant T/C snv 0.65 4
rs1184804
SLC17A3
0.925 0.120 6 25867998 intron variant T/A;C snv 4
rs1185567
SLC17A1
0.925 0.120 6 25818360 intron variant A/G;T snv 4
rs1185568
SLC17A3
0.925 0.120 6 25834200 intron variant T/A snv 0.65 4
rs1185569
SLC17A1
0.925 0.120 6 25831375 intron variant A/G snv 0.65 4
rs150551
CARMIL1
0.925 0.120 6 25533702 intron variant A/G;T snv 4
rs1540275 0.925 0.120 6 26036248 upstream gene variant T/A;C snv 4
rs1997672
CARMIL1
0.925 0.120 6 25617316 intron variant T/G snv 0.28 4
rs2051541 0.925 0.120 6 25944983 regulatory region variant A/G snv 0.47 4
rs2213284
H3C2
0.925 0.120 6 26031640 3 prime UTR variant G/A snv 0.70 0.76 4
rs3799352
SLC17A1
0.925 0.120 6 25822392 intron variant C/T snv 0.65 4
rs3804105
CARMIL1
0.925 0.120 6 25612455 intron variant A/C snv 0.29 4
rs6903765
CARMIL1
0.925 0.120 6 25609510 intron variant A/G;T snv 4
rs6905614
SLC17A3
0.925 0.120 6 25840257 intron variant C/A;G snv 4
rs6908390
CARMIL1
0.925 0.120 6 25609528 intron variant C/T snv 0.28 4
rs742132
CARMIL1
0.925 0.120 6 25607343 intron variant A/G snv 0.29 4
rs765285
SLC17A1
0.925 0.120 6 25828014 intron variant G/C;T snv 4
rs7761700
CARMIL1
0.925 0.120 6 25617963 intron variant G/C;T snv 4