rs3739696
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
9
Location
112454041
Variant Type
SNP
Genes
C9orf147
Phenotypes
ClinVar
Name
NM_032303.5(HSDL2):c.894A>G (p.Lys298=)
Allele
G
Clinical Significance
Benign