rs370169077 has not been reported to ClinVar. Refer to dbSNP record rs370169077 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: G
- Variation alleles: A, T
- Variation type: single nucleotide variation
- Organism: Homo sapiens
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GRCh38.p14: NC_000017.11: 7,221,554
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GRCh37.p13: NC_000017.10: 7,124,873
Genome Data Viewer
Source: KnownItemSensor
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Very long chain acyl-CoA dehydrogenase deficiency +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +2 more | |
Click to view in NCBI Gene