rs148207876
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
2
Location
3613349
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.169C>T (p.Arg57Trp)
Allele
T
Clinical Significance
Likely benign