rs2305256
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
6877890
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_080657.5(RSAD2):c.90G>A (p.Pro30=)
Allele
A
Clinical Significance
Benign
G
A
2
6877890
SNP
NM_080657.5(RSAD2):c.90G>A (p.Pro30=)
A
Benign