rs369567362
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
2
Location
3644046
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.744G>A (p.Ser248=)
Allele
A
Clinical Significance
Likely benign