rs762079957
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
1
Location
930336
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.791G>A (p.Arg264Lys)
Allele
A
Clinical Significance
Uncertain significance