rs1303270704
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
C
Chromosome
13
Location
38859400
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_207361.6(FREM2):c.7329T>A (p.Pro2443=)
Allele
A
Clinical Significance
Uncertain significance