rs764266
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
A
Chromosome
20
Location
10408832
Variant Type
SNP
Genes
ClinVar
Name
NM_170784.3(MKKS):c.986-29A>T
Allele
A
Clinical Significance
Benign
T
A
20
10408832
SNP
NM_170784.3(MKKS):c.986-29A>T
A
Benign