rs772007449
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
1
Location
930275
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.730T>G (p.Cys244Gly)
Allele
G
Clinical Significance
Uncertain significance