rs61733629
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
2
Location
219214414
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.1361T>C (p.Val454Ala)
Allele
G
Clinical Significance
Benign