Disease: Kallmann Syndrome 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs606231406
rs606231406
Entrez Id: 2798;550112
Gene Symbol: GNRHR;UBA6-AS1
GNRHR;UBA6-AS1
CUI: C1563719
Disease:
Kallmann Syndrome 1 		G 0.700 CausalMutation CLINVAR When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR). 22745237 2012