Variant (rsID / SNP)

rs182751201

rs182751201 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRM6. Location: chromosome 5, position 178,413,616. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GRM6Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 5:178413616
Cytoband: 5q35.3
HGVS: NM_000843.4(GRM6):c.1639C>T (p.Arg547Cys)
Allele change: Missense_R547C

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.