rs149202834
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
219217783
Variant Type
SNP
Genes
ClinVar
Name
NM_005689.4(ABCB6):c.574C>T (p.Arg192Trp)
Allele
A
Clinical Significance
Benign/Likely benign