rs199703563
- Benign/Likely benign
Your Genotype
Sign InDescription
This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.
This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.
Reference Allele
C
Alternative Allele
G
T
Chromosome
22
Location
37978057
Variant Type
SNP
ClinVar
Name
NM_006941.4(SOX10):c.507G>A (p.Pro169=)
Allele
T
Clinical Significance
Benign/Likely benign