Variant (rsID / SNP)
rs62542743
rs62542743 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AQP7. Location: chromosome 9, position 33,385,241. Clinical significance in the table: Affects.
Reference-table entries
AQP7Other
- Clinical significance (as recorded)
- Affects
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:33385241
- Cytoband
- 9p13.3
- HGVS
- NM_001170.1(AQP7):c.791G>T (p.Gly264Val)
- Allele change
- Silent
Associated conditions / phenotypes
Glycerol release during exercise, defective
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.