rs6984529
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
8
Location
69576064
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.267G>A (p.Pro89=)
Allele
A
Clinical Significance
Benign