rs145408226
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
G
Chromosome
2
Location
8750203
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020738.4(KIDINS220):c.3323A>G (p.Asn1108Ser)
Allele
C
Clinical Significance
Likely benign