rs113269917
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
2
Location
3604363
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.23T>C (p.Val8Ala)
Allele
C
Clinical Significance
Benign/Likely benign