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
rs57565032
EP400
12 131949846 upstream gene variant G/T snv 0.14 4
rs6000550
TMPRSS6
22 37067410 intron variant C/G;T snv 0.21 4
rs706027
BZW2
7 16660352 intron variant A/T snv 0.43 4
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
rs781191470
AXIN1
16 307744 intron variant G/A snv 3.1E-04 4
rs8013143
PSMB5
14 23025068 intron variant A/G snv 0.43 4
rs10414846
HAMP
19 35281568 intron variant C/T snv 0.21 3
rs116272812
CARMIL1
6 25452555 3 prime UTR variant T/C snv 8.1E-02 3
rs12712870
LOC105374567
2 42934040 intergenic variant A/G snv 0.57 3
rs13007705
ERFE
2 238160555 intron variant C/T snv 0.46 3
rs147428040
RBFOX2
22 36028975 upstream gene variant G/A snv 3.8E-02 3
rs17076726
CPEB4
5 173936886 intron variant C/T snv 0.43 3
rs17302154 2 196183605 intergenic variant A/C snv 9.8E-02 3
rs183034862
LOC102724081 ; CERS6
2 168457008 intron variant C/T snv 1.8E-02 3
rs2009581
ACOXL ; MIR4435-2HG
2 111050100 intron variant G/A snv 0.26 3
rs2468024
MTDH
8 97652425 intron variant G/A;C snv 3
rs2537594 7 17774912 intergenic variant G/A snv 0.58 3
rs2834259
ITSN1
21 33760786 intron variant C/T snv 0.30 3
rs34536858 19 35459272 intergenic variant A/G snv 0.33 3
rs3740685
RAPSN
11 47447239 intron variant C/T snv 0.59 3
rs4332427 10 24569461 intergenic variant A/G snv 0.21 3
rs56129102
CUL4A
13 113220766 intron variant C/T snv 0.20 3