Variant (rsID / SNP)

rs34797451

rs34797451 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RGS9. Location: chromosome 17, position 63,221,214. Clinical significance in the table: Benign.

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Reference-table entries

RGS9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:63221214
Cytoband: 17q24.1
HGVS: NM_003835.4(RGS9):c.1502G>A (p.Arg501His)
Allele change: Missense_R501H

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.