SLC12A7, solute carrier family 12 member 7, 10723

N. diseases: 31; N. variants: 14
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: rs4535497
rs4535497 		5 1107313 intron variant C/A snv 0.48
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2017 2017
dbSNP: rs56287436
rs56287436 		5 1080019 intron variant G/A snv 0.32
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2018 2018
dbSNP: rs56287436
rs56287436 		5 1080019 intron variant G/A snv 0.32
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2018 2018
dbSNP: rs6883412
rs6883412 		5 1093746 intron variant C/G;T snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs6883412
rs6883412 		5 1093746 intron variant C/G;T snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs55861694
rs55861694 		5 1051642 3 prime UTR variant A/C snv 1.1E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs55861694
rs55861694 		5 1051642 3 prime UTR variant A/C snv 1.1E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs13181874
rs13181874 		5 1112757 upstream gene variant G/C snv 0.44
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2016 2016
dbSNP: rs4580814
rs4580814 		5 1113129 upstream gene variant G/T snv 0.47
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2010 2010
dbSNP: rs4580814
rs4580814 		5 1113129 upstream gene variant G/T snv 0.47
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2010 2010