rs41280175
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
9
Location
112405714
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_032303.5(HSDL2):c.272A>T (p.Lys91Ile)
Allele
T
Clinical Significance
Benign
A
T
9
112405714
SNP
NM_032303.5(HSDL2):c.272A>T (p.Lys91Ile)
T
Benign