rs773032227
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
C
Alternative Allele
G
T
Chromosome
2
Location
3640310
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.307C>T (p.Pro103Ser)
Allele
T
Clinical Significance
Uncertain significance