rs76353556
- Benign
Your Genotype
Sign InDescription
Reference Allele
T
Alternative Allele
C
Chromosome
11
Location
65593838
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033347.2(KCNK7):c.356A>G (p.Lys119Arg)
Allele
C
Clinical Significance
Benign