rs1384741683
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
1
Location
942624
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1619C>A (p.Ala540Glu)
Allele
A
Clinical Significance
Uncertain significance