rs80215167
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
9
Location
112063019
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_022486.5(SUSD1):c.1768G>A (p.Glu590Lys)
Allele
T
Clinical Significance
Likely benign