rs2233915
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
9
Location
113256221
Variant Type
SNP
Genes
LOC107987119
Phenotypes
ClinVar
Name
NM_001859.4(SLC31A1):c.73C>G (p.Pro25Ala)
Allele
G
Clinical Significance
Benign