Disease: Wolf-Hirschhorn Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553873247
rs1553873247
Entrez Id: 7468
Gene Symbol: NSD2
NSD2
CUI: C1956097
Disease:
Wolf-Hirschhorn Syndrome 		T 0.700 CausalMutation CLINVAR