Variant (rsID / SNP)
rs640796
rs640796 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NXPE4. Location: chromosome 11, position 114,451,129. The table records no clinical significance for this variant.
Reference-table entries
NXPE4Not classified
- Variant type
- intron_variant
- Chromosome / position
- 11:114451129
- HGVS
- NM_001077639.2,c.893-69A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.