rs115672056
- Benign
Your Genotype
Sign InDescription
This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Reference Allele
T
Alternative Allele
A
C
Chromosome
2
Location
3558386
Variant Type
SNP
Genes
LOC100506054
Phenotypes
ClinVar
Name
NC_000002.12:g.3558386T>C
Allele
C
Clinical Significance
Benign