rs104894975
- Pathogenic
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
T
Chromosome
Y
Location
2787592
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_003140.3(SRY):c.12T>A (p.Tyr4Ter)
Allele
T
Clinical Significance
Pathogenic