rs548432777
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
8
Location
69601669
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.901G>A (p.Val301Met)
Allele
A
Clinical Significance
Uncertain significance