rs387906910
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
2
Location
219210036
Variant Type
SNP
ClinVar
Name
NM_005689.4(ABCB6):c.2431C>G (p.Leu811Val)
Allele
C
Clinical Significance
Pathogenic
G
C
2
219210036
SNP
NM_005689.4(ABCB6):c.2431C>G (p.Leu811Val)
C
Pathogenic