Disease: Red cell distribution width determination
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 11
rs77677521
MARCHF8
10 45457448 3 prime UTR variant C/G snv 1.3E-02 4
rs183034862
LOC102724081 ; CERS6
2 168457008 intron variant C/T snv 1.8E-02 3
rs72837788 6 24789643 downstream gene variant G/A snv 2.7E-02 3
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15
rs147428040
RBFOX2
22 36028975 upstream gene variant G/A snv 3.8E-02 3
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs2272783
FECH
1.000 18 57571588 synonymous variant A/G snv 0.12 6.3E-02 5
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs116272812
CARMIL1
6 25452555 3 prime UTR variant T/C snv 8.1E-02 3
rs73713131
TRAPPC9
8 140448235 intron variant T/C snv 8.8E-02 3
rs62064595 17 45383008 regulatory region variant A/G snv 9.8E-02 3
rs17302154 2 196183605 intergenic variant A/C snv 9.8E-02 3
rs920112
CDCA7
2 173354407 intron variant G/A snv 1.0E-01 5
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs741951
PTTG1IP
21 44849611 3 prime UTR variant G/A snv 0.14 4
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs57565032
EP400
12 131949846 upstream gene variant G/T snv 0.14 4
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs6068729 20 53931121 intergenic variant C/T snv 0.19 3