rs115731613
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
20
Location
9580619
Variant Type
SNP
Genes
PAK7
LOC105372523
Phenotypes
ClinVar
Name
NM_177990.4(PAK5):c.516A>G (p.Val172=)
Allele
C
Clinical Significance
Benign