rs16917454
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
112889585
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033051.4(SLC46A2):c.1097C>T (p.Ala366Val)
Allele
A
Clinical Significance
Benign