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
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs11244669
DHX32 ; BCCIP
10 125844213 intron variant A/C snv 0.28 4
rs116272812
CARMIL1
6 25452555 3 prime UTR variant T/C snv 8.1E-02 3
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03 4
rs1169299
HNF1A
1.000 0.080 12 120991391 intron variant T/C snv 0.43 4
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs12712870
LOC105374567
2 42934040 intergenic variant A/G snv 0.57 3
rs13007705
ERFE
2 238160555 intron variant C/T snv 0.46 3
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03 4
rs144204502
TK1 ; AFMID
17 78187152 5 prime UTR variant C/G;T snv 1.2E-02 4
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs147428040
RBFOX2
22 36028975 upstream gene variant G/A snv 3.8E-02 3
rs148125759
UGCG
9 111901105 intron variant T/C snv 1.0E-02 4
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs17076726
CPEB4
5 173936886 intron variant C/T snv 0.43 3
rs17302154 2 196183605 intergenic variant A/C snv 9.8E-02 3
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs183034862
LOC102724081 ; CERS6
2 168457008 intron variant C/T snv 1.8E-02 3