rs77339398
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
9
Location
112409029
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032303.5(HSDL2):c.395+8T>C
Allele
C
Clinical Significance
Benign
T
C
9
112409029
SNP
NM_032303.5(HSDL2):c.395+8T>C
C
Benign