rs571654307
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
1
Location
941284
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1336G>A (p.Ala446Thr)
Allele
A
Clinical Significance
Conflicting interpretations of pathogenicity