rs1641882544
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
1
Location
942938
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1933A>G (p.Arg645Gly)
Allele
G
Clinical Significance
Uncertain significance