rs41285790
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
1
Location
930248
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.703G>A (p.Gly235Ser)
Allele
A
Clinical Significance
Likely benign