Variant (rsID / SNP)
rs10501986
rs10501986 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPC6. Location: chromosome 11, position 101,375,549. Clinical significance in the table: Benign.
Reference-table entries
TRPC6Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:101375549
- Cytoband
- 11q22.1
- HGVS
- NM_004621.6(TRPC6):c.171-20A>G
- Allele change
- Silent
Associated conditions / phenotypes
Focal segmental glomerulosclerosis 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.