rs17829458
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
Chromosome
9
Location
112142425
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_022486.5(SUSD1):c.601C>G (p.Gln201Glu)
Allele
C
Clinical Significance
Likely benign