Variant (rsID / SNP)

rs143491269

rs143491269 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRM6. Location: chromosome 5, position 178,413,684. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

GRM6Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 5:178413684
Cytoband: 5q35.3
HGVS: NM_000843.4(GRM6):c.1571C>T (p.Pro524Leu)
Allele change: Missense_P524L

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.