Variant (rsID / SNP)
rs75841704
rs75841704 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDLIM5. Location: chromosome 4, position 95,376,504. The table records no clinical significance for this variant.
Reference-table entries
PDLIM5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 4:95376504
- HGVS
- NM_001256426.2,c.65A>G,p.Lys22Arg
- Allele change
- Silent
Associated conditions / phenotypes
Missense_K22R|Missense_K22R|Missense_K22R|Silent|Missense_K22R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.