Variant (rsID / SNP)

rs869025214

rs869025214 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM6. Location: chromosome 9, position 77,403,529. Clinical significance in the table: Pathogenic.

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Reference-table entries

TRPM6Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:77403529
Cytoband: 9q21.13
HGVS: NM_017662.5(TRPM6):c.2667+1G>A
Allele change: Silent

Associated conditions / phenotypes

Intestinal hypomagnesemia 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.