rs141185224, RET

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 10 43114681 missense variant G/A snv 1.1E-04 7.7E-05 0.010 1.000 1 2004 2004
Ovarian Failure, Premature
CUI: C0085215
Disease: Ovarian Failure, Premature
115 0.925 0.080 10 43114681 missense variant G/A snv 1.1E-04 7.7E-05 0.010 1.000 1 2004 2004