rs2228592
- Benign
Your Genotype
Sign InDescription
Reference Allele
A
Alternative Allele
G
Chromosome
8
Location
70128448
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_006540.4(NCOA2):c.3666T>C (p.Pro1222=)
Allele
G
Clinical Significance
Benign
A
G
8
70128448
SNP
NM_006540.4(NCOA2):c.3666T>C (p.Pro1222=)
G
Benign