rs137852660, FGF8

N. diseases: 3
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 6 WITH OR WITHOUT ANOSMIA
CUI: C3552574
Disease: HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA
10 0.882 0.160 10 101775209 missense variant G/A snv 1.1E-03 8.0E-04 0.800 1.000 2 2008 2013
Kallmann Syndrome
CUI: C0162809
Disease: Kallmann Syndrome
30 0.882 0.160 10 101775209 missense variant G/A snv 1.1E-03 8.0E-04 0.010 1 2014 2014
VATER/VACTERL ASSOCIATION
CUI: C4225671
Disease: VATER/VACTERL ASSOCIATION
2 0.882 0.160 10 101775209 missense variant G/A snv 1.1E-03 8.0E-04 0.010 1.000 1 2014 2014