Variant (rsID / SNP)

rs2274924

rs2274924 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRPM6. Location: chromosome 9, position 77,376,647. Clinical significance in the table: Benign.

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Reference-table entries

TRPM6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:77376647
Cytoband: 9q21.13
HGVS: NM_017662.5(TRPM6):c.4750A>G (p.Lys1584Glu)
Allele change: Missense_K1579E

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.