rs190528998
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
2
Location
219216781
Variant Type
SNP
Genes
ClinVar
Name
NM_005689.4(ABCB6):c.739C>T (p.Arg247Cys)
Allele
A
Clinical Significance
Benign
G
A
T
2
219216781
SNP
NM_005689.4(ABCB6):c.739C>T (p.Arg247Cys)
A
Benign