Variant (rsID / SNP)

rs2292191

rs2292191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RPF1. Location: chromosome 1, position 84,944,989. The table records no clinical significance for this variant.

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Reference-table entries

RPF1Not classified

Variant type: missense_variant
Chromosome / position: 1:84944989
HGVS: NM_025065.7,c.25A>G,p.Ser9Gly
Allele change: Missense_S9G

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.