rs1363663761
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
16
Location
2090479
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12250C>T (p.Pro4084Ser)
Allele
A
Clinical Significance
Likely benign