rs4512367
- association
Your Genotype
Sign InDescription
The frequency of the homozygous WT and SNP genotypes was higher in the oral cancer patients in comparison to controls implying the role of this genotype in predisposition of oral cancer while the heterozygous genotype frequency was higher in controls indicating decreased risk to oral cancer.
Reference Allele
C
Alternative Allele
G
T
Chromosome
8
Location
68015357
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024870.4(PREX2):c.142-2489C>T
Allele
T
Clinical Significance
association