rs61747130
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
8
Location
69624136
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.1789A>G (p.Arg597Gly)
Allele
G
Clinical Significance
Benign