rs376664522
- Affects
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
219212413
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.1942C>T (p.Arg648Ter)
Allele
A
Clinical Significance
Affects