rs1377097612
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
Chromosome
2
Location
219211077
Variant Type
SNP
Genes
ClinVar
Name
NM_005689.4(ABCB6):c.2000G>C (p.Gly667Ala)
Allele
G
Clinical Significance
Uncertain significance