rs2031920 has not been reported to ClinVar. Refer to dbSNP record rs2031920 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 allele: T
- Variation type: single nucleotide variation
- Organism: Homo sapiens
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GRCh38.p14: NC_000010.11: 133,526,340
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GRCh37.p13: NC_000010.10: 135,339,844
Genome Data Viewer
Source: KnownItemSensor
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant | CYP2E1*5B ALLELE | |
| | | Single nucleotide variant | Not Specified | Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant |
Click to view in NCBI Gene