rs2091438383
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
16
Location
2090364
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12365G>A (p.Trp4122Ter)
Allele
T
Clinical Significance
Pathogenic