rs148386909
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
T
Chromosome
1
Location
935895
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.966C>G (p.Ala322=)
Allele
G
Clinical Significance
Uncertain significance