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
rs56129102
CUL4A
13 113220766 intron variant C/T snv 0.20 3
rs57565032
EP400
12 131949846 upstream gene variant G/T snv 0.14 4
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs595982
PPP1R15A
19 48874988 synonymous variant T/C snv 0.33 0.39 3
rs6000550
TMPRSS6
22 37067410 intron variant C/G;T snv 0.21 4
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs6068729 20 53931121 intergenic variant C/T snv 0.19 3
rs6084653
SMOX
20 4176425 intron variant C/G;T snv 3
rs62064595 17 45383008 regulatory region variant A/G snv 9.8E-02 3
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5
rs706027
BZW2
7 16660352 intron variant A/T snv 0.43 4
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs72837788 6 24789643 downstream gene variant G/A snv 2.7E-02 3
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs73713131
TRAPPC9
8 140448235 intron variant T/C snv 8.8E-02 3
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs741951
PTTG1IP
21 44849611 3 prime UTR variant G/A snv 0.14 4
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
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
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs7789162
H2AZ2
7 44833301 intron variant T/C snv 0.48 3