rs267608676
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
C
T
Chromosome
10
Location
78009539
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.1907C>A (p.Ser636Tyr)
Allele
T
Clinical Significance
Pathogenic