rs17851586
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
G
Chromosome
2
Location
6877925
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_080657.5(RSAD2):c.125T>G (p.Leu42Arg)
Allele
G
Clinical Significance
Benign
T
G
2
6877925
SNP
NM_080657.5(RSAD2):c.125T>G (p.Leu42Arg)
G
Benign