rs748736842
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
2
Location
3643735
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.433G>A (p.Gly145Ser)
Allele
A
Clinical Significance
Uncertain significance