rs374783198
- Likely benign
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
Chromosome
13
Location
39655810
Variant Type
SNP
Genes
ClinVar
Name
NM_020751.3(COG6):c.84G>A (p.Ser28=)
Allele
A
Clinical Significance
Likely benign
Name
NM_020751.3(COG6):c.84G>C (p.Ser28=)
Allele
C
Clinical Significance
Likely benign