rs1564620047
- Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
10
Location
78009646
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.1800C>T (p.Ile600=)
Allele
A
Clinical Significance
Likely pathogenic