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: rs2067087
rs2067087
Entrez Id: 3209;100316868
Gene Symbol: HOXA13;HOTTIP
HOXA13;HOTTIP
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The results showed three SNPs (rs3807598, rs2067087, and rs17427960) were associated with enhanced CRC risk both in overall and stratified analysis. 30940774 2019