rs1188292999
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
T
Chromosome
16
Location
2090375
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12354C>A (p.Tyr4118Ter)
Allele
T
Clinical Significance
Pathogenic