rs111474126
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
8
Location
69589076
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.669G>T (p.Ala223=)
Allele
T
Clinical Significance
Benign/Likely benign