rs368865, ATP11A

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
RDW - Red blood cell distribution width result
988 13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 0.700 1.000 2 2017 2019
Red cell distribution width determination
988 13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 0.700 1.000 2 2017 2019
Finding of Mean Corpuscular Hemoglobin
1206 13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 0.700 1.000 1 2019 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 0.700 1.000 1 2019 2019