Disease: Red cell distribution width determination
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs3756668
PIK3R1
0.925 0.160 5 68300260 3 prime UTR variant G/A;C snv 3
rs4332427 10 24569461 intergenic variant A/G snv 0.21 3
rs56129102
CUL4A
13 113220766 intron variant C/T snv 0.20 3
rs595982
PPP1R15A
19 48874988 synonymous variant T/C snv 0.33 0.39 3
rs6068729 20 53931121 intergenic variant C/T snv 0.19 3
rs6084653
SMOX
20 4176425 intron variant C/G;T snv 3
rs62064595 17 45383008 regulatory region variant A/G snv 9.8E-02 3
rs72837788 6 24789643 downstream gene variant G/A snv 2.7E-02 3
rs73713131
TRAPPC9
8 140448235 intron variant T/C snv 8.8E-02 3
rs7789162
H2AZ2
7 44833301 intron variant T/C snv 0.48 3
rs78694551
GPR75-ASB3 ; ASB3
2 53751676 intron variant A/G;T snv 3