rs369831329, 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.
Hypogonadism
CUI: C0020619
Disease: Hypogonadism
24 0.925 0.160 20 5302374 missense variant A/T snv 8.0E-06 0.010 1.000 1 2013 2013
Kallmann Syndrome
CUI: C0162809
Disease: Kallmann Syndrome
30 0.925 0.160 20 5302374 missense variant A/T snv 8.0E-06 0.010 1.000 1 2013 2013