rs148458820
- Affects
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219216803
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.717G>A (p.Trp239Ter)
Allele
T
Clinical Significance
Affects