ROGDI, rogdi atypical leucine zipper, 79641

N. diseases: 61; N. variants: 12
Disease: Cerebral white matter atrophy ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907145
rs387907145
Entrez Id: 79641
Gene Symbol: ROGDI
ROGDI
CUI: C4022735
Disease:
Cerebral white matter atrophy 		A 0.700 CausalMutation CLINVAR