FGG, fibrinogen gamma chain, 2266

N. diseases: 70; N. variants: 18
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: rs148685782
rs148685782 		1.000 0.080 4 154611883 missense variant G/C snv 1.9E-03 2.2E-03
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2016 2016
dbSNP: rs2066861
rs2066861 		4 154606284 intron variant C/T snv 0.26
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2011 2011