rs76755084
- Benign
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
11
Location
65593867
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_033347.2(KCNK7):c.327C>T (p.Gly109=)
Allele
A
Clinical Significance
Benign
G
A
11
65593867
SNP
NM_033347.2(KCNK7):c.327C>T (p.Gly109=)
A
Benign