rs754667801
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219216027
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.1124G>A (p.Arg375Gln)
Allele
T
Clinical Significance
Pathogenic