rs397514756
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
2
Location
219216084
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.1067T>C (p.Leu356Pro)
Allele
G
Clinical Significance
Pathogenic