Variant (rsID / SNP)

rs17078894

rs17078894 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRM6. Location: chromosome 5, position 178,418,555. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GRM6Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:178418555
Cytoband: 5q35.3
HGVS: NM_000843.4(GRM6):c.727G>T (p.Val243Phe)
Allele change: Missense_V243F

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.