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
rs920112
CDCA7
2 173354407 intron variant G/A snv 1.0E-01 5
rs17076726
CPEB4
5 173936886 intron variant C/T snv 0.43 3
rs2537594 7 17774912 intergenic variant G/A snv 0.58 3
rs17302154 2 196183605 intergenic variant A/C snv 9.8E-02 3
rs9850274 3 196195556 downstream gene variant A/G snv 0.76 3
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 7
rs8013143
PSMB5
14 23025068 intron variant A/G snv 0.43 4
rs13007705
ERFE
2 238160555 intron variant C/T snv 0.46 3
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs4332427 10 24569461 intergenic variant A/G snv 0.21 3
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs72837788 6 24789643 downstream gene variant G/A snv 2.7E-02 3
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs116272812
CARMIL1
6 25452555 3 prime UTR variant T/C snv 8.1E-02 3
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs781191470
AXIN1
16 307744 intron variant G/A snv 3.1E-04 4
rs9392465 6 3162144 upstream gene variant C/A snv 0.57 3
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs2834259
ITSN1
21 33760786 intron variant C/T snv 0.30 3
rs10414846
HAMP
19 35281568 intron variant C/T snv 0.21 3
rs34536858 19 35459272 intergenic variant A/G snv 0.33 3
rs147428040
RBFOX2
22 36028975 upstream gene variant G/A snv 3.8E-02 3