rs764893806
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
219216028
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.1123C>T (p.Arg375Trp)
Allele
A
Clinical Significance
Pathogenic