rs1590917647
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
11
Location
65641288
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_006747.4(SIPA1):c.367A>G (p.Ser123Gly)
Allele
G
Clinical Significance
Uncertain significance