rs749362185
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
8
Location
69603253
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.1123G>A (p.Asp375Asn)
Allele
A
Clinical Significance
Uncertain significance