rs538017286
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
69586473
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.529G>A (p.Gly177Ser)
Allele
A
Clinical Significance
Likely benign