rs72556578
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
T
Chromosome
11
Location
65649965
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_006747.4(SIPA1):c.2762G>T (p.Gly921Val)
Allele
T
Clinical Significance
Benign