rs7021942
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
9
Location
112889905
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033051.4(SLC46A2):c.777T>C (p.Asp259=)
Allele
G
Clinical Significance
Benign
A
G
9
112889905
SNP
NM_033051.4(SLC46A2):c.777T>C (p.Asp259=)
G
Benign