rs147107178
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
113260425
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001859.4(SLC31A1):c.525C>T (p.Phe175=)
Allele
T
Clinical Significance
Benign