Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2286503
rs2286503
TOMM7
7 22816987 intron variant C/T snv 0.48
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.800 1.000 1 2013 2013
dbSNP: rs71520386
rs71520386
TOMM7
7 22813902 intron variant C/T snv 0.13
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay 		0.700 1.000 1 2016 2016