rs775757190
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
C
T
Chromosome
22
Location
37973816
Variant Type
SNP
Phenotypes
ClinVar
Name
NM_006941.4(SOX10):c.1080C>T (p.Thr360=)
Allele
A
Clinical Significance
Benign
G
A
C
T
22
37973816
SNP
NM_006941.4(SOX10):c.1080C>T (p.Thr360=)
A
Benign