rs34351135
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
3643475
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.360G>A (p.Lys120=)
Allele
A
Clinical Significance
Benign
G
A
2
3643475
SNP
NM_024027.5(COLEC11):c.360G>A (p.Lys120=)
A
Benign