RS121908102 CYP27A1

Health Risk Chr 2:218813094 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Cholestanol storage disease
CYP27A1-related disorder
Cardiovascular phenotype
Cholestanol storage disease
CYP27A1-related disorder
Cardiovascular phenotype
Population Frequencies
gnomAD ALL
0%
1kG AFR
100%
1kG ALL
0%
1kG AMR
100%
1kG EAS
0.1%
1kG EUR
100%
1kG SAS
100%
Other Variants in CYP27A1
rs72551322 rs121908096 rs397515353 rs397515354 rs121908097 rs121908098 rs121908099 rs397515355 rs72551313 rs397515356
Ask Dr. Hemsworth about this variant