rs189368660
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
19
Location
7632826
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_174895.3(PCP2):c.56G>T (p.Gly19Val)
Allele
A
Clinical Significance
Benign
C
A
19
7632826
SNP
NM_174895.3(PCP2):c.56G>T (p.Gly19Val)
A
Benign