rs34159261
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
8
Location
70596318
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_014294.6(TRAM1):c.430A>G (p.Asn144Asp)
Allele
C
Clinical Significance
Benign
T
C
8
70596318
SNP
NM_014294.6(TRAM1):c.430A>G (p.Asn144Asp)
C
Benign