Variant (rsID / SNP)
rs2303138
rs2303138 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LNPEP. Location: chromosome 5, position 96,350,710. The table records no clinical significance for this variant.
Reference-table entries
LNPEPNot classified
- Variant type
- missense_variant
- Chromosome / position
- 5:96350710
- HGVS
- NM_005575.3,c.2287G>A,p.Ala763Thr
- Allele change
- Missense_A763T
Associated conditions / phenotypes
Pustulosis of Palm and Sole|Psoriasis|Patent Ductus Venosus|Psoriasis 1|Hellp Syndrome|Pre-Eclampsia|Eclampsia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.