rs150937195
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
11
Location
65649380
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006747.4(SIPA1):c.2425C>T (p.His809Tyr)
Allele
T
Clinical Significance
Benign
C
T
11
65649380
SNP
NM_006747.4(SIPA1):c.2425C>T (p.His809Tyr)
T
Benign