rs7022287
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
9
Location
112889923
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033051.4(SLC46A2):c.759C>T (p.Tyr253=)
Allele
A
Clinical Significance
Benign