rs483352876
- not provided
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219213280
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.1766G>A (p.Arg589His)
Allele
T
Clinical Significance
not provided