rs114822090
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
9
Location
112889956
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033051.4(SLC46A2):c.726C>T (p.Ala242=)
Allele
A
Clinical Significance
Benign