rs770894660
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
1
Location
942987
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1982G>A (p.Gly661Glu)
Allele
A
Clinical Significance
Uncertain significance