rs748564095
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
2
Location
8731470
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020738.4(KIDINS220):c.4566C>T (p.Asp1522=)
Allele
A
Clinical Significance
Likely benign