rs375443308
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
16
Location
2089804
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12835C>A (p.Arg4279=)
Allele
T
Clinical Significance
Likely benign