rs1565191003
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
T
Chromosome
11
Location
65659665
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_021975.4(RELA):c.559+1G>A
Allele
T
Clinical Significance
Pathogenic
C
T
11
65659665
SNP
NM_021975.4(RELA):c.559+1G>A
T
Pathogenic