rs774063520
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
C
Alternative Allele
G
T
Chromosome
8
Location
69576167
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001128205.2(SULF1):c.370C>T (p.Arg124Trp)
Allele
T
Clinical Significance
Uncertain significance