rs796065353
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
2
Location
219213495
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.1663C>A (p.Gln555Lys)
Allele
T
Clinical Significance
Pathogenic