rs150221689
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219217782
Variant Type
SNP
Genes
ClinVar
Name
NM_005689.4(ABCB6):c.575G>A (p.Arg192Gln)
Allele
T
Clinical Significance
Benign/Likely benign