rs1641861059
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
1
Location
942692
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1687C>G (p.Leu563Val)
Allele
G
Clinical Significance
Uncertain significance