Variant (rsID / SNP)

rs889248

rs889248 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RGS7BP. Location: chromosome 5, position 63,905,068. The table records no clinical significance for this variant.

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Reference-table entries

RGS7BPNot classified

Variant type: missense_variant
Chromosome / position: 5:63905068
HGVS: NM_001029875.3,c.763A>G,p.Ile255Val
Allele change: Missense_I255V

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.