rs137852589 has not been reported to ClinVar. Refer to dbSNP record rs137852589 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, T
- Variation type: single nucleotide variation
- Organism: Homo sapiens
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GRCh38.p14: NC_000023.11: 67,721,856
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GRCh37.p13: NC_000023.10: 66,941,698
Genome Data Viewer
Source: KnownItemSensor
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Androgen resistance syndrome | |
| | | Single nucleotide variant (missense variant) | Androgen resistance syndrome | |
Click to view in NCBI Gene