rs1862514
- Benign
Your Genotype
Sign InDescription
Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: MAF
Reference Allele
C
Alternative Allele
T
Chromosome
19
Location
7633434
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_174895.3(PCP2):c.24G>A (p.Thr8=)
Allele
T
Clinical Significance
Benign