rs864309710 has not been reported to ClinVar. Refer to dbSNP record rs864309710 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
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GRCh38.p14: NC_000001.11: 160,323,446
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GRCh37.p13: NC_000001.10: 160,293,236
Genome Data Viewer
Source: KnownItemSensor
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Autoimmune interstitial lung disease-arthritis syndrome | |
| | | Single nucleotide variant (missense variant) | Autoimmune interstitial lung disease-arthritis syndrome | |
Click to view in NCBI Gene