rs114406044
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
2
Location
8682268
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_002166.5(ID2):c.103C>T (p.Leu35=)
Allele
T
Clinical Significance
Benign
C
G
T
2
8682268
SNP
NM_002166.5(ID2):c.103C>T (p.Leu35=)
T
Benign