rs2091453268
- Pathogenic
Your Genotype
Sign InDescription
PVS1, PM1,PP4
Reference Allele
T
Alternative Allele
G
Chromosome
16
Location
2090592
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12139-2A>C
Allele
G
Clinical Significance
Pathogenic