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Variant (rsID / SNP)

rs10891705

NXPE4

rs10891705 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NXPE4. Location: chromosome 11, position 114,441,943. The table records no clinical significance for this variant.

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Reference-table entries

NXPE4Not classified
Variant type
missense_variant
Chromosome / position
11:114441943
HGVS
NM_001077639.2,c.1352C>T,p.Ala451Val
Allele change
Missense_A167V

Public references

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