rs146410593
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
219216841
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_005689.4(ABCB6):c.688-9C>T
Allele
A
Clinical Significance
Benign
G
A
2
219216841
SNP
NM_005689.4(ABCB6):c.688-9C>T
A
Benign