rs766567862
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
2
Location
8734724
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020738.4(KIDINS220):c.3747G>A (p.Gln1249=)
Allele
T
Clinical Significance
Likely benign