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
rs78694551
GPR75-ASB3 ; ASB3
2 53751676 intron variant A/G;T snv 3
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs706027
BZW2
7 16660352 intron variant A/T snv 0.43 4
rs9392465 6 3162144 upstream gene variant C/A snv 0.57 3
rs79674254
AK9
6 109501078 intron variant C/A;T snv 3
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs77677521
MARCHF8
10 45457448 3 prime UTR variant C/G snv 1.3E-02 4
rs888194 12 109549113 downstream gene variant C/G snv 0.50 3
rs144204502
TK1 ; AFMID
17 78187152 5 prime UTR variant C/G;T snv 1.2E-02 4
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs6000550
TMPRSS6
22 37067410 intron variant C/G;T snv 0.21 4
rs6084653
SMOX
20 4176425 intron variant C/G;T snv 3
rs10414846
HAMP
19 35281568 intron variant C/T snv 0.21 3
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 15
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs13007705
ERFE
2 238160555 intron variant C/T snv 0.46 3
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs17076726
CPEB4
5 173936886 intron variant C/T snv 0.43 3
rs183034862
LOC102724081 ; CERS6
2 168457008 intron variant C/T snv 1.8E-02 3
rs2834259
ITSN1
21 33760786 intron variant C/T snv 0.30 3
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs3740685
RAPSN
11 47447239 intron variant C/T snv 0.59 3
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12