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Variant (rsID / SNP)

rs2292819

NXPE4

rs2292819 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NXPE4. Location: chromosome 11, position 114,452,339. The table records no clinical significance for this variant.

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Reference-table entries

NXPE4Not classified
Variant type
intron_variant
Chromosome / position
11:114452339
HGVS
NM_001077639.2,c.892+108C>T
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.