rs2091436717
- Uncertain significance
Your Genotype
Sign InDescription
PM2, PP3, PP4
Reference Allele
A
Alternative Allele
C
Chromosome
16
Location
2090343
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12386T>G (p.Met4129Arg)
Allele
C
Clinical Significance
Uncertain significance