rs372534935
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
16
Location
2090492
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12237C>T (p.Ser4079=)
Allele
A
Clinical Significance
Likely benign