rs374138625
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
3640294
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.291C>T (p.Ser97=)
Allele
T
Clinical Significance
Benign
C
T
2
3640294
SNP
NM_024027.5(COLEC11):c.291C>T (p.Ser97=)
T
Benign