rs147151457
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
9
Location
112078557
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_022486.5(SUSD1):c.1734C>T (p.Ser578=)
Allele
A
Clinical Significance
Likely benign