rs75316826
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
20
Location
9544431
Variant Type
SNP
Genes
PAK7
Phenotypes
ClinVar
Name
NM_177990.4(PAK5):c.1807T>C (p.Leu603=)
Allele
G
Clinical Significance
Benign