rs1064797205
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
16
Location
2089956
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12683G>C (p.Arg4228Pro)
Allele
G
Clinical Significance
Likely pathogenic