rs115339119
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
112157606
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_022486.5(SUSD1):c.111C>T (p.Asp37=)
Allele
A
Clinical Significance
Benign
G
A
9
112157606
SNP
NM_022486.5(SUSD1):c.111C>T (p.Asp37=)
A
Benign