rs1160476310
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
1
Location
942216
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1439T>G (p.Phe480Cys)
Allele
G
Clinical Significance
Uncertain significance