rs184866499
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
8751481
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_020738.4(KIDINS220):c.3175C>T (p.Arg1059Trp)
Allele
A
Clinical Significance
Benign