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
rs595982
PPP1R15A
19 48874988 synonymous variant T/C snv 0.33 0.39 3
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
rs72837788 6 24789643 downstream gene variant G/A snv 2.7E-02 3
rs73713131
TRAPPC9
8 140448235 intron variant T/C snv 8.8E-02 3
rs7789162
H2AZ2
7 44833301 intron variant T/C snv 0.48 3
rs78694551
GPR75-ASB3 ; ASB3
2 53751676 intron variant A/G;T snv 3
rs79674254
AK9
6 109501078 intron variant C/A;T snv 3
rs888194 12 109549113 downstream gene variant C/G snv 0.50 3
rs9392465 6 3162144 upstream gene variant C/A snv 0.57 3
rs9394841
CCND3
6 41959197 intron variant T/C snv 0.22 3
rs9423289
C10orf88
10 122945179 intron variant C/T snv 0.58 3
rs9850274 3 196195556 downstream gene variant A/G snv 0.76 3
rs9972293
C15orf41
15 36578054 upstream gene variant T/C snv 0.37 3