rs34436491
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
3643481
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.366C>T (p.Ile122=)
Allele
T
Clinical Significance
Benign
C
T
2
3643481
SNP
NM_024027.5(COLEC11):c.366C>T (p.Ile122=)
T
Benign