rs1553305119
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
2
Location
8731984
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020738.4(KIDINS220):c.4054-2A>G
Allele
C
Clinical Significance
Uncertain significance