rs888350690
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
8
Location
69576161
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.364G>T (p.Glu122Ter)
Allele
T
Clinical Significance
Uncertain significance