rs111852229
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
2
Location
219214964
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.1273C>G (p.Leu425Val)
Allele
C
Clinical Significance
Likely benign