SPTB, spectrin beta, erythrocytic, 6710

N. diseases: 66; N. variants: 34
Disease: SPHEROCYTOSIS, HEREDITARY, 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555369657
rs1555369657
Entrez Id: 6710;102465841
Gene Symbol: SPTB;MIR7855
SPTB;MIR7855
CUI: C2674219
Disease:
SPHEROCYTOSIS, HEREDITARY, 2 		A 0.700 CausalMutation CLINVAR