LAMA5, laminin subunit alpha 5, 3911

N. diseases: 56; N. variants: 9
Disease: Familial hematuria ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs756101090
rs756101090
Entrez Id: 3911
Gene Symbol: LAMA5
LAMA5
CUI: C1305904
Disease:
Familial hematuria 		A 0.700 CausalMutation CLINVAR