rs11859517, CHD9

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 16 53147335 intron variant C/T snv 0.28 0.700 1.000 1 2016 2016