Source: ALL

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: rs112069438
rs112069438
TXNDC11
16 11733034 intron variant G/A snv 2.1E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs6498239
rs6498239
TXNDC11
16 11686918 intron variant T/C snv 0.54
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs6498239
rs6498239
TXNDC11
16 11686918 intron variant T/C snv 0.54
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs78784853
rs78784853
TXNDC11
16 11723610 intron variant A/C snv 6.4E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9924009
rs9924009
TXNDC11
16 11688193 intron variant G/A;T snv
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2015 2015
dbSNP: rs9924009
rs9924009
TXNDC11
16 11688193 intron variant G/A;T snv
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015