Variant (rsID / SNP)
rs34523089
rs34523089 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RNF43. Location: chromosome 17, position 56,436,109. The table records no clinical significance for this variant.
Reference-table entries
RNF43Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:56436109
- HGVS
- NM_001305544.2,c.1028G>A,p.Arg343His
- Allele change
- Missense_R343H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.