rs80360485
- not provided
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
16
Location
2090556
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_001009944.3(PKD1):c.12173T>G (p.Val4058Gly)
Allele
C
Clinical Significance
not provided