rs57467915
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
219216694
Variant Type
SNP
Genes
ClinVar
Name
NM_005689.4(ABCB6):c.826C>T (p.Arg276Trp)
Allele
A
Clinical Significance
Benign
G
A
2
219216694
SNP
NM_005689.4(ABCB6):c.826C>T (p.Arg276Trp)
A
Benign