rs142148202
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
69601656
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.888G>A (p.Leu296=)
Allele
A
Clinical Significance
Benign