rs786205631
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
2
Location
3603614
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.-26-701G>C
Allele
C
Clinical Significance
Uncertain significance