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
rs6068729 20 53931121 intergenic variant C/T snv 0.19 3
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs9423289
C10orf88
10 122945179 intron variant C/T snv 0.58 3
rs147428040
RBFOX2
22 36028975 upstream gene variant G/A snv 3.8E-02 3
rs2009581
ACOXL ; MIR4435-2HG
2 111050100 intron variant G/A snv 0.26 3
rs2537594 7 17774912 intergenic variant G/A snv 0.58 3
rs532591337 19 12459271 intron variant G/A snv 4.9E-05 4
rs72837788 6 24789643 downstream gene variant G/A snv 2.7E-02 3
rs741951
PTTG1IP
21 44849611 3 prime UTR variant G/A snv 0.14 4
rs781191470
AXIN1
16 307744 intron variant G/A snv 3.1E-04 4
rs920112
CDCA7
2 173354407 intron variant G/A snv 1.0E-01 5
rs2468024
MTDH
8 97652425 intron variant G/A;C snv 3
rs3756668
PIK3R1
0.925 0.160 5 68300260 3 prime UTR variant G/A;C snv 5
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 7
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs57565032
EP400
12 131949846 upstream gene variant G/T snv 0.14 4
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03 4
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 7
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11