rs779619427
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
1
Location
930317
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.772A>G (p.Ile258Val)
Allele
G
Clinical Significance
Uncertain significance