rs60956063
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
9
Location
112080173
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_022486.5(SUSD1):c.1475-8C>T
Allele
A
Clinical Significance
Benign
G
A
9
112080173
SNP
NM_022486.5(SUSD1):c.1475-8C>T
A
Benign