rs1231644914
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
13
Location
38784805
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.6016G>C (p.Asp2006His)
Allele
C
Clinical Significance
Uncertain significance