RS10509681 CYP2C8

Health Risk Chr 10:95038991 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"This is a CYP2C8 SNP. The CYP2C8*3 allele is mapped to both rs10509681 and rs11572080). In a 2009 ar...
Associated Conditions
Pulmonary disease
chronic obstructive
susceptibility to
CYP2C8-related disorder
Pulmonary disease
chronic obstructive
susceptibility to
CYP2C8-related disorder
Population Frequencies
gnomAD ALL
89.4%
1kG AFR
0.8%
1kG ALL
4.6%
1kG AMR
90.1%
1kG EAS
0.1%
1kG EUR
11.8%
1kG SAS
3%
Other Variants in CYP2C8
rs72558196 rs1934953 rs3752988
Ask Dr. Hemsworth about this variant