rs1168641193
- Pathogenic/Likely pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
A
Chromosome
10
Location
78029405
Variant Type
SNP
Genes
ClinVar
Name
NM_007055.4(POLR3A):c.3G>T (p.Met1Ile)
Allele
A
Clinical Significance
Pathogenic/Likely pathogenic