rs138672528, PROKR2

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.
HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA
CUI: C3550478
Disease: HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA
20 0.925 0.160 20 5314027 missense variant C/T snv 3.2E-05 7.0E-06 0.700 0
Kallmann Syndrome
CUI: C0162809
Disease: Kallmann Syndrome
30 0.925 0.160 20 5314027 missense variant C/T snv 3.2E-05 7.0E-06 0.010 1.000 1 2008 2008