rs201816303
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
9
Location
112098537
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_022486.5(SUSD1):c.1407G>T (p.Val469=)
Allele
A
Clinical Significance
Likely benign