rs397507554
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
2
Location
3575889
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001011.4(RPS7):c.147+1G>A
Allele
A
Clinical Significance
Pathogenic
G
A
2
3575889
SNP
NM_001011.4(RPS7):c.147+1G>A
A
Pathogenic