rs397514483
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
C
Chromosome
20
Location
9409166
Variant Type
SNP
Genes
ClinVar
Name
NM_001377142.1(PLCB4):c.1984A>C (p.Asn662His)
Allele
C
Clinical Significance
Pathogenic