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
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs17302154 2 196183605 intergenic variant A/C snv 9.8E-02 3
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs2537594 7 17774912 intergenic variant G/A snv 0.58 3
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs34536858 19 35459272 intergenic variant A/G snv 0.33 3
rs4332427 10 24569461 intergenic variant A/G snv 0.21 3
rs532591337 19 12459271 intron variant G/A snv 4.9E-05 4
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs6068729 20 53931121 intergenic variant C/T snv 0.19 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
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs739385 7 93053295 regulatory region variant G/A;C snv 4
rs888194 12 109549113 downstream gene variant C/G snv 0.50 3
rs9392465 6 3162144 upstream gene variant C/A snv 0.57 3
rs9850274 3 196195556 downstream gene variant A/G snv 0.76 3
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs2009581
ACOXL ; MIR4435-2HG
2 111050100 intron variant G/A snv 0.26 3
rs79674254
AK9
6 109501078 intron variant C/A;T snv 3
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs368865
ATP11A
13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 4
rs781191470
AXIN1
16 307744 intron variant G/A snv 3.1E-04 4