HOXA13, homeobox A13, 3209

N. diseases: 126; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17501292
rs17501292
Entrez Id: 3209;100316868
Gene Symbol: HOXA13;HOTTIP
HOXA13;HOTTIP
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE One polymorphism, rs17501292, could improve the overall survival (OS) of CRC patients in the tumor of ulcerative/invasive-type subgroup. 30940774 2019