rs397514757
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
2
Location
219218166
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.508A>G (p.Ser170Gly)
Allele
C
Clinical Significance
Pathogenic