rs1640863258
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
1
Location
925952
Variant Type
SNP
Genes
LOC107985728
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.548G>A (p.Gly183Glu)
Allele
A
Clinical Significance
Uncertain significance