MSX1, msh homeobox 1, 4487

N. diseases: 180; N. variants: 21
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8670
rs8670
Entrez Id: 4487
Gene Symbol: MSX1
MSX1
CUI: C1306459
Disease:
Primary malignant neoplasm
0.010 GeneticVariation BEFREE However, the T allele and T carrier (TC + CC) of rs12532 and rs8670 showed no association with cancer susceptibility. 25501212 2014