rs3760675
- 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
19
Location
7629776
Variant Type
SNP
Phenotypes
ClinVar
Name
NC_000019.10:g.7629776T>C
Allele
C
Clinical Significance
Benign