Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs41313381
rs41313381
1 78946283 missense variant C/A;T snv 1.9E-02; 3.3E-05
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs41313381
rs41313381
1 78946283 missense variant C/A;T snv 1.9E-02; 3.3E-05
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs41313381
rs41313381
1 78946283 missense variant C/A;T snv 1.9E-02; 3.3E-05
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs41313381
rs41313381
1 78946283 missense variant C/A;T snv 1.9E-02; 3.3E-05
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019