rs148211042
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219210799
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.2168G>A (p.Arg723Gln)
Allele
T
Clinical Significance
Uncertain significance