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
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 6
rs9411378
ABO
9 133270015 intron variant A/C;T snv 5
rs12459419
CD33
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31 4
rs1958078
SMOC1
14 69888141 intron variant A/C;G snv 4
rs4619875
TIGD4 ; ARFIP1
4 152779978 5 prime UTR variant C/G;T snv 3
rs7260330 19 44932959 downstream gene variant A/G snv 0.39 3
rs9801017
TFR2
7 100638579 intron variant G/A snv 0.65 3