rs7934094, TTC17

N. diseases: 1
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 11 43484157 intron variant T/G snv 0.15 0.700 1.000 2 2016 2017