rs143390223
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
112143473
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_022486.5(SUSD1):c.524C>T (p.Thr175Ile)
Allele
A
Clinical Significance
Benign