rs1568763104
- Pathogenic
- Conflicting interpretations of pathogenicity
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
20
Location
9409106
Variant Type
SNP
Genes
ClinVar
Name
NM_001377142.1(PLCB4):c.1924G>T (p.Asp642Tyr)
Allele
T
Clinical Significance
Pathogenic
Name
NM_001377142.1(PLCB4):c.1924G>A (p.Asp642Asn)
Allele
A
Clinical Significance
Conflicting interpretations of pathogenicity