rs118056333
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
8
Location
69603241
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.1111A>G (p.Ile371Val)
Allele
G
Clinical Significance
Benign/Likely benign