rs35971725
- Benign
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
11
Location
65570646
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006396.3(ZNRD2):c.62C>T (p.Thr21Met)
Allele
T
Clinical Significance
Benign
C
G
T
11
65570646
SNP
NM_006396.3(ZNRD2):c.62C>T (p.Thr21Met)
T
Benign