SATB2, SATB homeobox 2, 23314

N. diseases: 233; N. variants: 38
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553544133
rs1553544133
Entrez Id: 23314
Gene Symbol: SATB2
SATB2
CUI: C1850049
Disease:
Clinodactyly of the 5th finger
C 0.700 CausalMutation CLINVAR