F2, coagulation factor II, thrombin, 2147

N. diseases: 490; N. variants: 42
Disease: Tonometry ×
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: rs5896
rs5896 		0.882 0.160 11 46723453 missense variant C/G;T snv 0.21
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018