rs199706529 has not been reported to ClinVar. Refer to dbSNP record rs199706529 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, C
- Variation type: single nucleotide variation
- Organism: Homo sapiens
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GRCh38.p14: NC_000004.12: 101,083,202
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GRCh37.p13: NC_000004.11: 102,004,359
Genome Data Viewer
Source: KnownItemSensor
| Variation | | Type (Consequence) | Condition | Classification, Review status |
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| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Epileptic encephalopathy, infantile or early childhood, 1 | |
Click to view in NCBI Gene