rs149363094
- Benign/Likely benign
Your Genotype
Sign InDescription
See Variant Classification Assertion Criteria.
Reference Allele
G
Alternative Allele
A
C
Chromosome
2
Location
219213842
Variant Type
SNP
Genes
ClinVar
Name
NM_005689.4(ABCB6):c.1562C>G (p.Thr521Ser)
Allele
C
Clinical Significance
Benign/Likely benign