rs6730396
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
2
Location
3701529
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_018436.4(ALLC):c.868T>C (p.Cys290Arg)
Allele
C
Clinical Significance
Benign
T
C
2
3701529
SNP
NM_018436.4(ALLC):c.868T>C (p.Cys290Arg)
C
Benign