Variant (rsID / SNP)

rs3847193

rs3847193 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to QRFP. Location: chromosome 9, position 133,769,169. The table records no clinical significance for this variant.

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Reference-table entries

QRFPNot classified

Variant type: synonymous_variant
Chromosome / position: 9:133769169
HGVS: NM_198180.3,c.57C>T,p.Phe19Phe
Allele change: Synonymous_F19F

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.