rs4134809
- 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
G
Alternative Allele
A
C
T
Chromosome
19
Location
7629507
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_020196.3(XAB2):c.21C>T (p.Leu7=)
Allele
A
Clinical Significance
Benign