PDCD5, programmed cell death 5, 9141

N. diseases: 67; N. variants: 5
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10405535
rs10405535
19 32581179 upstream gene variant A/G;T snv
Red cell distribution width determination
0.700 1.000 2 2016 2017
dbSNP: rs10405535
rs10405535
19 32581179 upstream gene variant A/G;T snv
RDW - Red blood cell distribution width result
0.700 1.000 2 2016 2017
dbSNP: rs4499344
rs4499344
19 32582525 intron variant G/A snv 0.46
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 2 2018 2018
dbSNP: rs10402931
rs10402931
19 32581163 upstream gene variant G/A;C;T snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs4499344
rs4499344
19 32582525 intron variant G/A snv 0.46
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs4499344
rs4499344
19 32582525 intron variant G/A snv 0.46
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs71176136
rs71176136
19 32579739 upstream gene variant AA/-;A;AAA delins 0.78
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs71351177
rs71351177
19 32581408 intron variant G/C snv 2.2E-02
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs71351177
rs71351177
19 32581408 intron variant G/C snv 2.2E-02
Red cell distribution width determination
0.700 1.000 1 2019 2019