rs146843448
- Likely benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
9
Location
112041911
Variant Type
SNP
Genes
LOC105376220
Phenotypes
ClinVar
Name
NM_022486.5(SUSD1):c.2199G>A (p.Leu733=)
Allele
T
Clinical Significance
Likely benign