rs10170348
- Benign
Your Genotype
Sign InDescription
Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
3626058
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_024027.5(COLEC11):c.203-11475G>A
Allele
A
Clinical Significance
Benign