DNM2, dynamin 2, 1785

N. diseases: 178; N. variants: 30
Disease: Henoch-Schoenlein Purpura ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs757334523
rs757334523
Entrez Id: 1785;102466737
Gene Symbol: DNM2;MIR6793
DNM2;MIR6793
CUI: C0034152
Disease:
Henoch-Schoenlein Purpura 		0.010 GeneticVariation BEFREE Awareness of this distinct association between HSP and c.2155C > T, p.R719W mutation will facilitate ascertainment of additional DNM2 HSP families and will direct future research toward better understanding of cell biological processes involved in these partly overlapping clinical syndromes. 26517984 2015