Variant (rsID / SNP)
rs41268472
rs41268472 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LCE4A. Location: chromosome 1, position 152,681,603. The table records no clinical significance for this variant.
Reference-table entries
LCE4ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:152681603
- HGVS
- NM_001387222.1,c.52A>G,p.Ile18Val
- Allele change
- Missense_I18V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.