rs13402964
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
T
Chromosome
2
Location
219212412
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.1943G>A (p.Arg648Gln)
Allele
T
Clinical Significance
Likely benign