rs1574808120
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
2
Location
219210235
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.2415G>A (p.Arg805=)
Allele
T
Clinical Significance
Likely benign