rs17058957
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
13
Location
39012840
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_025138.5(PROSER1):c.2412C>T (p.Pro804=)
Allele
A
Clinical Significance
Benign