rs778531580
- Uncertain significance
Your Genotype
Sign InDescription
This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Reference Allele
G
Alternative Allele
A
T
Chromosome
13
Location
38846654
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.6101G>T (p.Gly2034Val)
Allele
T
Clinical Significance
Uncertain significance