rs759210811
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
16
Location
2090153
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12486C>A (p.Pro4162=)
Allele
T
Clinical Significance
Likely benign