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
rs11244669
DHX32 ; BCCIP
10 125844213 intron variant A/C snv 0.28 4
rs17302154 2 196183605 intergenic variant A/C snv 9.8E-02 3
rs2857078
SLC4A1
17 44252803 intron variant A/C snv 0.62 4
rs1958078
SMOC1
14 69888141 intron variant A/C;G snv 4
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs368865
ATP11A
13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 4
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03 4
rs12712870
LOC105374567
2 42934040 intergenic variant A/G snv 0.57 3
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs2272783
FECH
1.000 18 57571588 synonymous variant A/G snv 0.12 6.3E-02 4
rs3208787
NPLOC4
17 81558634 3 prime UTR variant A/G snv 0.24 4
rs34536858 19 35459272 intergenic variant A/G snv 0.33 3
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs35893164
PIM1
6 37175357 3 prime UTR variant A/G snv 6.5E-03 4
rs4332427 10 24569461 intergenic variant A/G snv 0.21 3
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs62064595 17 45383008 regulatory region variant A/G snv 9.8E-02 3
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 5
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs8013143
PSMB5
14 23025068 intron variant A/G snv 0.43 4
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs9850274 3 196195556 downstream gene variant A/G snv 0.76 3
rs11756659 6 25933704 upstream gene variant A/G;T snv 4