rs79578215
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
2
Location
219169529
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001144889.2(SLC23A3):c.312G>C (p.Met104Ile)
Allele
G
Clinical Significance
Benign