rs3837091, DDC

N. diseases: 2
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.
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 1.000 7 50561043 5 prime UTR variant TCTC/-;TC delins 0.23 0.010 1.000 1 2013 2013
Hypotension, Orthostatic
CUI: C0020651
Disease: Hypotension, Orthostatic
21 1.000 7 50561043 5 prime UTR variant TCTC/-;TC delins 0.23 0.010 1.000 1 2019 2019