SLC22A4, solute carrier family 22 member 4, 6583

N. diseases: 90; N. variants: 21
Disease: Fibrinogen assay ×
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: rs12777
rs12777 		5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.800 1.000 2 2009 2016
dbSNP: rs10479002
rs10479002 		5 132335969 synonymous variant C/G snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2009 2009
dbSNP: rs270607
rs270607 		5 132313493 intron variant A/G snv 0.69
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2011 2011