Variant (rsID / SNP)
rs12948507
rs12948507 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RFNG. Location: chromosome 17, position 80,006,957. The table records no clinical significance for this variant.
Reference-table entries
RFNGNot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:80006957
- HGVS
- NM_002917.2,c.864T>G,p.His288Gln
- Allele change
- Missense_H288Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.