rs764447736
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
16
Location
2090338
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12391G>T (p.Glu4131Ter)
Allele
A
Clinical Significance
Pathogenic