rs1176956891
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
1
Location
942648
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1643A>G (p.Asn548Ser)
Allele
G
Clinical Significance
Uncertain significance