rs11572080 has not been reported to ClinVar. Refer to dbSNP record rs11572080 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar
Genetic variation
- Clinical significance: not reported in ClinVar
- Reference allele: C
- Variation alleles: A, T
- Variation type: single nucleotide variation
- Organism: Homo sapiens
-
GRCh38.p14: NC_000010.11: 95,067,272
-
GRCh37.p13: NC_000010.10: 96,827,029
Genome Data Viewer
Source: KnownItemSensor
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | CYP2C8 HAPLOTYPE POLYMORPHISM | |
| | | Single nucleotide variant (missense variant) | CYP2C8-related condition | |
Click to view in NCBI Gene