rs1641861633
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
1
Location
942701
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001385641.1(SAMD11):c.1696G>C (p.Gly566Arg)
Allele
C
Clinical Significance
Uncertain significance