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: rs10512597
rs10512597 		17 74703694 intron variant T/A;C snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.800 1.000 3 2009 2017
dbSNP: rs35489971
rs35489971 		1.000 0.040 17 74704804 missense variant A/G;T snv 0.73
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2017 2017