rs767385060
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
16
Location
2089836
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12803C>T (p.Pro4268Leu)
Allele
A
Clinical Significance
Uncertain significance