Disease: Red Blood Cell Count measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 8
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 6
rs2032447
H3C3 ; H2BC3 ; H2AC5P
0.925 0.120 6 26044141 non coding transcript exon variant A/G snv 4.1E-06; 0.67 0.67 6
rs7756117
H3C3
0.882 0.160 6 26046337 upstream gene variant G/A snv 0.69 6
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs129129
TRIM38
0.925 0.120 6 25960801 upstream gene variant A/G snv 0.73 5
rs13129697
SLC2A9
0.925 0.120 4 9925343 intron variant T/G snv 0.39 5
rs1540276
H4C2
0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs198853
H4C3
0.925 0.120 6 26103868 upstream gene variant T/C snv 0.28 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5