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
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs1865760
SLC17A2
0.925 0.120 6 25916751 synonymous variant C/T snv 0.42 0.34 5
rs6415788
GLIS3
9 4118111 missense variant G/T snv 0.67 0.62 4
rs6918725
LOC105377992
6 126669246 intron variant T/G snv 0.50 4
rs74929147 19 18302251 downstream gene variant G/A;C snv 4
rs117642368 17 45321692 upstream gene variant G/C snv 6.9E-02 3
rs36225153
OTUD4
4 145160700 intron variant C/T snv 9.9E-02 3
rs531184891
KDM2A
11 67129907 intron variant AA/-;A;AAA delins 5.0E-02 3
rs6484504
DNAJC24
11 31403276 intron variant T/C snv 0.79 3
rs7952436
KDM2A
11 67257063 3 prime UTR variant C/T snv 4.7E-02 3
rs10165255
CYS1
2 10059474 intron variant A/G snv 0.59 2
rs12614953 2 43194322 intergenic variant T/C snv 0.44 2
rs12661188
L3MBTL3
6 130057688 intron variant T/A;C snv 2
rs1319012
USP49
6 41884878 intron variant T/A snv 0.94 2
rs3020623
SERPINE1
7 101129564 intron variant G/A snv 0.32 2
rs5745297
DAP
5 10680885 missense variant G/A snv 5.5E-02 5.7E-02 2
rs679228
ACTN3
11 66556951 intron variant C/T snv 0.45 2
rs7557989
THADA
2 43403518 intron variant C/T snv 0.34 2
rs865923
LOC105371566 ; MYO15A
17 18151603 intron variant T/A;C snv 2
rs9841945 3 157863678 intron variant T/C snv 0.69 2