Variant (rsID / SNP)

rs17078877

rs17078877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRM6. Location: chromosome 5, position 178,410,213. Clinical significance in the table: Benign.

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Reference-table entries

GRM6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:178410213
Cytoband: 5q35.3
HGVS: NM_000843.4(GRM6):c.2134A>G (p.Met712Val)
Allele change: Missense_M712V

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.