rs772542835
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
2
Location
8731719
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020738.4(KIDINS220):c.4317T>C (p.Ser1439=)
Allele
G
Clinical Significance
Likely benign