rs75861149
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
11
Location
65645074
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_006747.4(SIPA1):c.1104C>T (p.Gly368=)
Allele
T
Clinical Significance
Benign
C
T
11
65645074
SNP
NM_006747.4(SIPA1):c.1104C>T (p.Gly368=)
T
Benign