rs116498125
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
6883444
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_080657.5(RSAD2):c.420G>A (p.Val140=)
Allele
A
Clinical Significance
Benign
G
A
2
6883444
SNP
NM_080657.5(RSAD2):c.420G>A (p.Val140=)
A
Benign