rs1553305080
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
8731898
Variant Type
SNP
Genes
ClinVar
Name
NM_020738.4(KIDINS220):c.4138C>T (p.Gln1380Ter)
Allele
A
Clinical Significance
Likely pathogenic