rs369572769, LAMA5

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.
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.925 0.080 20 62312259 missense variant C/T snv 2.5E-05 1.4E-05 0.010 1.000 1 2017 2017
Nyctalopia
CUI: C0028077
Disease: Nyctalopia
18 0.925 0.080 20 62312259 missense variant C/T snv 2.5E-05 1.4E-05 0.010 1.000 1 2017 2017