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
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
rs739385 7 93053295 regulatory region variant G/A;C snv 4
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
rs77677521
MARCHF8
10 45457448 3 prime UTR variant C/G snv 1.3E-02 4
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs7789162
H2AZ2
7 44833301 intron variant T/C snv 0.48 3
rs781191470
AXIN1
16 307744 intron variant G/A snv 3.1E-04 4
rs78694551
GPR75-ASB3 ; ASB3
2 53751676 intron variant A/G;T snv 3
rs79674254
AK9
6 109501078 intron variant C/A;T snv 3
rs8013143
PSMB5
14 23025068 intron variant A/G snv 0.43 4
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 7
rs888194 12 109549113 downstream gene variant C/G snv 0.50 3
rs920112
CDCA7
2 173354407 intron variant G/A snv 1.0E-01 5
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
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
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
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
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88