rs147479634
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
8
Location
69621049
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.1392T>G (p.Ile464Met)
Allele
G
Clinical Significance
Benign