rs749087938
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
G
Chromosome
16
Location
2090270
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12444+15G>C
Allele
G
Clinical Significance
Likely benign