Variant (rsID / SNP)
rs2274925
rs2274925 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM6. Location: chromosome 9, position 77,376,633. Clinical significance in the table: Benign.
Reference-table entries
TRPM6Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 9:77376633
- Cytoband
- 9q21.13
- HGVS
- NM_017662.5(TRPM6):c.4764T>C (p.Asn1588=)
- Allele change
- Synonymous_N1583N
Associated conditions / phenotypes
Intestinal hypomagnesemia 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.