rs387906911
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
2
Location
219218505
Variant Type
SNP
Genes
ClinVar
Name
NM_005689.4(ABCB6):c.169G>A (p.Ala57Thr)
Allele
T
Clinical Significance
Pathogenic
C
T
2
219218505
SNP
NM_005689.4(ABCB6):c.169G>A (p.Ala57Thr)
T
Pathogenic