rs7940495
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
11
Location
65570520
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006396.3(ZNRD2):c.19+10T>C
Allele
C
Clinical Significance
Benign
T
C
11
65570520
SNP
NM_006396.3(ZNRD2):c.19+10T>C
C
Benign