rs121909041 has not been reported to ClinVar. Refer to dbSNP record rs121909041 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: T
- Variation alleles: A, C
- Variation type: single nucleotide variation
- Organism: Homo sapiens
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GRCh38.p14: NC_000007.14: 117,642,482
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GRCh37.p13: NC_000007.13: 117,282,536
Genome Data Viewer
Source: KnownItemSensor
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Cystic fibrosis +1 more | GPathogenic; drug response |
Click to view in NCBI Gene