rs199913532
- Benign/Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
8747956
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020738.4(KIDINS220):c.3459C>T (p.Gly1153=)
Allele
A
Clinical Significance
Benign/Likely benign