rs112123068
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
8
Location
69604926
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.1371G>A (p.Pro457=)
Allele
A
Clinical Significance
Benign