Variant (rsID / SNP)

rs9916764

rs9916764 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RFNG, GPS1. Location: chromosome 17, position 80,008,392. The table records no clinical significance for this variant.

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Reference-table entries

RFNGNot classified

Variant type: synonymous_variant
Chromosome / position: 17:80008392
HGVS: NM_002917.2,c.459C>A,p.Ala153Ala
Allele change: Synonymous_A153A

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.